http://rdf.disgenet.org/resource/nanopub/NP956896.RAD3WFhC4qkeEPysHhpIlWT-sM3LhVcyym3aKLvYkX_4M#head
http://rdf.disgenet.org/resource/nanopub/NP956896.RAD3WFhC4qkeEPysHhpIlWT-sM3LhVcyym3aKLvYkX_4M
http://www.nanopub.org/nschema#hasAssertion
http://rdf.disgenet.org/resource/nanopub/NP956896.RAD3WFhC4qkeEPysHhpIlWT-sM3LhVcyym3aKLvYkX_4M#assertion
http://rdf.disgenet.org/resource/nanopub/NP956896.RAD3WFhC4qkeEPysHhpIlWT-sM3LhVcyym3aKLvYkX_4M
http://www.nanopub.org/nschema#hasProvenance
http://rdf.disgenet.org/resource/nanopub/NP956896.RAD3WFhC4qkeEPysHhpIlWT-sM3LhVcyym3aKLvYkX_4M#provenance
http://rdf.disgenet.org/resource/nanopub/NP956896.RAD3WFhC4qkeEPysHhpIlWT-sM3LhVcyym3aKLvYkX_4M
http://www.nanopub.org/nschema#hasPublicationInfo
http://rdf.disgenet.org/resource/nanopub/NP956896.RAD3WFhC4qkeEPysHhpIlWT-sM3LhVcyym3aKLvYkX_4M#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP956896.RAD3WFhC4qkeEPysHhpIlWT-sM3LhVcyym3aKLvYkX_4M
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://www.nanopub.org/nschema#Nanopublication
http://rdf.disgenet.org/resource/nanopub/NP956896.RAD3WFhC4qkeEPysHhpIlWT-sM3LhVcyym3aKLvYkX_4M#assertion
http://rdf.disgenet.org/resource/gda/DGNce091bf6f2176d467a624d566d79b32e
http://semanticscience.org/resource/SIO_000628
http://identifiers.org/ncbigene/6559
http://rdf.disgenet.org/resource/gda/DGNce091bf6f2176d467a624d566d79b32e
http://semanticscience.org/resource/SIO_000628
http://linkedlifedata.com/resource/umls/id/C0268450
http://rdf.disgenet.org/resource/gda/DGNce091bf6f2176d467a624d566d79b32e
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://semanticscience.org/resource/SIO_001122
http://rdf.disgenet.org/resource/nanopub/NP956896.RAD3WFhC4qkeEPysHhpIlWT-sM3LhVcyym3aKLvYkX_4M#provenance
http://rdf.disgenet.org/resource/nanopub/NP956896.RAD3WFhC4qkeEPysHhpIlWT-sM3LhVcyym3aKLvYkX_4M#assertion
http://purl.org/dc/terms/description
[Neonatal Bartter's syndrome is caused by mutations of NKCC2 or ROMK, classic Bartter's syndrome by mutations of ClC-Kb, Bartter's syndrome associated with sensorineural deafness is due to mutations of BSND, Gitelman's syndrome to mutations of NCCT and Bartter's syndrome associated with autosomal dominant hypocalcemia is linked to mutations of CASR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
http://rdf.disgenet.org/resource/nanopub/NP956896.RAD3WFhC4qkeEPysHhpIlWT-sM3LhVcyym3aKLvYkX_4M#assertion
http://purl.org/ontology/wi/core#evidence
http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature
http://rdf.disgenet.org/resource/nanopub/NP956896.RAD3WFhC4qkeEPysHhpIlWT-sM3LhVcyym3aKLvYkX_4M#assertion
http://semanticscience.org/resource/SIO_000772
http://identifiers.org/pubmed/15056980
http://rdf.disgenet.org/resource/nanopub/NP956896.RAD3WFhC4qkeEPysHhpIlWT-sM3LhVcyym3aKLvYkX_4M#assertion
http://www.w3.org/ns/prov#wasDerivedFrom
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://rdf.disgenet.org/resource/nanopub/NP956896.RAD3WFhC4qkeEPysHhpIlWT-sM3LhVcyym3aKLvYkX_4M#assertion
http://www.w3.org/ns/prov#wasGeneratedBy
http://purl.obolibrary.org/obo/ECO_0000203
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://purl.org/pav/importedOn
2017-02-19
http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.obolibrary.org/obo/ECO_0000212
http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature
http://www.w3.org/2000/01/rdf-schema#comment
Gene-disease associations inferred from text-mining the literature.
http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature
http://www.w3.org/2000/01/rdf-schema#label
DisGeNET evidence - LITERATURE
http://rdf.disgenet.org/resource/nanopub/NP956896.RAD3WFhC4qkeEPysHhpIlWT-sM3LhVcyym3aKLvYkX_4M#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP956896.RAD3WFhC4qkeEPysHhpIlWT-sM3LhVcyym3aKLvYkX_4M
http://purl.org/dc/terms/created
2017-10-17T13:16:17+02:00
http://rdf.disgenet.org/resource/nanopub/NP956896.RAD3WFhC4qkeEPysHhpIlWT-sM3LhVcyym3aKLvYkX_4M
http://purl.org/dc/terms/rights
http://opendatacommons.org/licenses/odbl/1.0/
http://rdf.disgenet.org/resource/nanopub/NP956896.RAD3WFhC4qkeEPysHhpIlWT-sM3LhVcyym3aKLvYkX_4M
http://purl.org/dc/terms/rightsHolder
http://rdf.disgenet.org/v5.0.0/void/IBIGroup
http://rdf.disgenet.org/resource/nanopub/NP956896.RAD3WFhC4qkeEPysHhpIlWT-sM3LhVcyym3aKLvYkX_4M
http://purl.org/dc/terms/subject
http://semanticscience.org/resource/SIO_000983
http://rdf.disgenet.org/resource/nanopub/NP956896.RAD3WFhC4qkeEPysHhpIlWT-sM3LhVcyym3aKLvYkX_4M
http://purl.org/net/provenance/ns#usedData
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://rdf.disgenet.org/resource/nanopub/NP956896.RAD3WFhC4qkeEPysHhpIlWT-sM3LhVcyym3aKLvYkX_4M
http://purl.org/pav/authoredBy
http://orcid.org/0000-0001-5999-6269
http://rdf.disgenet.org/resource/nanopub/NP956896.RAD3WFhC4qkeEPysHhpIlWT-sM3LhVcyym3aKLvYkX_4M
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-7534-7661
http://rdf.disgenet.org/resource/nanopub/NP956896.RAD3WFhC4qkeEPysHhpIlWT-sM3LhVcyym3aKLvYkX_4M
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-9383-528X
http://rdf.disgenet.org/resource/nanopub/NP956896.RAD3WFhC4qkeEPysHhpIlWT-sM3LhVcyym3aKLvYkX_4M
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP956896.RAD3WFhC4qkeEPysHhpIlWT-sM3LhVcyym3aKLvYkX_4M
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-1244-7654
http://rdf.disgenet.org/resource/nanopub/NP956896.RAD3WFhC4qkeEPysHhpIlWT-sM3LhVcyym3aKLvYkX_4M
http://purl.org/pav/createdBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP956896.RAD3WFhC4qkeEPysHhpIlWT-sM3LhVcyym3aKLvYkX_4M
http://purl.org/pav/version
v5.0.0.0
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://purl.org/pav/version
v5.0.0