http://rdf.disgenet.org/resource/nanopub/NP616104.RAFJd0EMJg63lLucpJgbQlITY96SrALh23O96VfiAQC3I#head
http://rdf.disgenet.org/resource/nanopub/NP616104.RAFJd0EMJg63lLucpJgbQlITY96SrALh23O96VfiAQC3I
http://www.nanopub.org/nschema#hasAssertion
http://rdf.disgenet.org/resource/nanopub/NP616104.RAFJd0EMJg63lLucpJgbQlITY96SrALh23O96VfiAQC3I#assertion
http://rdf.disgenet.org/resource/nanopub/NP616104.RAFJd0EMJg63lLucpJgbQlITY96SrALh23O96VfiAQC3I
http://www.nanopub.org/nschema#hasProvenance
http://rdf.disgenet.org/resource/nanopub/NP616104.RAFJd0EMJg63lLucpJgbQlITY96SrALh23O96VfiAQC3I#provenance
http://rdf.disgenet.org/resource/nanopub/NP616104.RAFJd0EMJg63lLucpJgbQlITY96SrALh23O96VfiAQC3I
http://www.nanopub.org/nschema#hasPublicationInfo
http://rdf.disgenet.org/resource/nanopub/NP616104.RAFJd0EMJg63lLucpJgbQlITY96SrALh23O96VfiAQC3I#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP616104.RAFJd0EMJg63lLucpJgbQlITY96SrALh23O96VfiAQC3I
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://www.nanopub.org/nschema#Nanopublication
http://rdf.disgenet.org/resource/nanopub/NP616104.RAFJd0EMJg63lLucpJgbQlITY96SrALh23O96VfiAQC3I#assertion
http://rdf.disgenet.org/resource/gda/DGN8fd78a2dadcad1747c254f812ec9f5b6
http://semanticscience.org/resource/SIO_000628
http://identifiers.org/ncbigene/3767
http://rdf.disgenet.org/resource/gda/DGN8fd78a2dadcad1747c254f812ec9f5b6
http://semanticscience.org/resource/SIO_000628
http://linkedlifedata.com/resource/umls/id/C0011847
http://rdf.disgenet.org/resource/gda/DGN8fd78a2dadcad1747c254f812ec9f5b6
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://semanticscience.org/resource/SIO_001122
http://rdf.disgenet.org/resource/nanopub/NP616104.RAFJd0EMJg63lLucpJgbQlITY96SrALh23O96VfiAQC3I#provenance
http://rdf.disgenet.org/resource/nanopub/NP616104.RAFJd0EMJg63lLucpJgbQlITY96SrALh23O96VfiAQC3I#assertion
http://purl.org/dc/terms/description
[It has been known for some time that loss of function mutations in KCNJ11, which encodes for Kir6.2, and ABCC8, which encodes for SUR1, can cause oversecretion of insulin and result in hyperinsulinism of infancy, while activating mutations in KCNJ11 and ABCC8 have recently been described that result in the opposite phenotype of diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
http://rdf.disgenet.org/resource/nanopub/NP616104.RAFJd0EMJg63lLucpJgbQlITY96SrALh23O96VfiAQC3I#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/NP616104.RAFJd0EMJg63lLucpJgbQlITY96SrALh23O96VfiAQC3I#assertion
http://semanticscience.org/resource/SIO_000772
http://identifiers.org/pubmed/18767144
http://rdf.disgenet.org/resource/nanopub/NP616104.RAFJd0EMJg63lLucpJgbQlITY96SrALh23O96VfiAQC3I#assertion
http://www.w3.org/ns/prov#wasDerivedFrom
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://rdf.disgenet.org/resource/nanopub/NP616104.RAFJd0EMJg63lLucpJgbQlITY96SrALh23O96VfiAQC3I#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/NP616104.RAFJd0EMJg63lLucpJgbQlITY96SrALh23O96VfiAQC3I#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP616104.RAFJd0EMJg63lLucpJgbQlITY96SrALh23O96VfiAQC3I
http://purl.org/dc/terms/created
2017-10-17T13:14:06+02:00
http://rdf.disgenet.org/resource/nanopub/NP616104.RAFJd0EMJg63lLucpJgbQlITY96SrALh23O96VfiAQC3I
http://purl.org/dc/terms/rights
http://opendatacommons.org/licenses/odbl/1.0/
http://rdf.disgenet.org/resource/nanopub/NP616104.RAFJd0EMJg63lLucpJgbQlITY96SrALh23O96VfiAQC3I
http://purl.org/dc/terms/rightsHolder
http://rdf.disgenet.org/v5.0.0/void/IBIGroup
http://rdf.disgenet.org/resource/nanopub/NP616104.RAFJd0EMJg63lLucpJgbQlITY96SrALh23O96VfiAQC3I
http://purl.org/dc/terms/subject
http://semanticscience.org/resource/SIO_000983
http://rdf.disgenet.org/resource/nanopub/NP616104.RAFJd0EMJg63lLucpJgbQlITY96SrALh23O96VfiAQC3I
http://purl.org/net/provenance/ns#usedData
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://rdf.disgenet.org/resource/nanopub/NP616104.RAFJd0EMJg63lLucpJgbQlITY96SrALh23O96VfiAQC3I
http://purl.org/pav/authoredBy
http://orcid.org/0000-0001-5999-6269
http://rdf.disgenet.org/resource/nanopub/NP616104.RAFJd0EMJg63lLucpJgbQlITY96SrALh23O96VfiAQC3I
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-7534-7661
http://rdf.disgenet.org/resource/nanopub/NP616104.RAFJd0EMJg63lLucpJgbQlITY96SrALh23O96VfiAQC3I
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-9383-528X
http://rdf.disgenet.org/resource/nanopub/NP616104.RAFJd0EMJg63lLucpJgbQlITY96SrALh23O96VfiAQC3I
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP616104.RAFJd0EMJg63lLucpJgbQlITY96SrALh23O96VfiAQC3I
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-1244-7654
http://rdf.disgenet.org/resource/nanopub/NP616104.RAFJd0EMJg63lLucpJgbQlITY96SrALh23O96VfiAQC3I
http://purl.org/pav/createdBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP616104.RAFJd0EMJg63lLucpJgbQlITY96SrALh23O96VfiAQC3I
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