@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP1018043.RAiR8ewoWLCvSy96VQiJgV9FcZADKRhbB99obFT4czltw130_head { this: np:hasAssertion dgn-np:NP1018043.RAiR8ewoWLCvSy96VQiJgV9FcZADKRhbB99obFT4czltw130_assertion ; np:hasProvenance dgn-np:NP1018043.RAiR8ewoWLCvSy96VQiJgV9FcZADKRhbB99obFT4czltw130_provenance ; np:hasPublicationInfo dgn-np:NP1018043.RAiR8ewoWLCvSy96VQiJgV9FcZADKRhbB99obFT4czltw130_publicationInfo ; a np:Nanopublication . dgn-np:NP1018043.RAiR8ewoWLCvSy96VQiJgV9FcZADKRhbB99obFT4czltw130_assertion a np:Assertion . dgn-np:NP1018043.RAiR8ewoWLCvSy96VQiJgV9FcZADKRhbB99obFT4czltw130_provenance a np:Provenance . dgn-np:NP1018043.RAiR8ewoWLCvSy96VQiJgV9FcZADKRhbB99obFT4czltw130_publicationInfo a np:PublicationInfo . } dgn-np:NP1018043.RAiR8ewoWLCvSy96VQiJgV9FcZADKRhbB99obFT4czltw130_assertion { miriam-gene:102723996 a ncit:C16612 . lld:C0009324 a ncit:C7057 . dgn-gda:DGN7eefd2007a5c53815e0e8664cb0093f5 sio:SIO_000628 miriam-gene:102723996 , lld:C0009324 ; a sio:SIO_001122 . } dgn-np:NP1018043.RAiR8ewoWLCvSy96VQiJgV9FcZADKRhbB99obFT4czltw130_provenance { dgn-np:NP1018043.RAiR8ewoWLCvSy96VQiJgV9FcZADKRhbB99obFT4czltw130_assertion dcterms:description "[In the subphenotype meta-analysis, rs1738074-TAGAP (P=7.40 × 10(-5), OR: 0.61), rs6974491-ELMO1 (P=0.00052, OR: 1.73) and rs4819388-ICOSLG (P=0.00019, OR: 0.75) associated with familial UC, pediatric UC and sporadic UC, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ; wi:evidence dgn-void:source_evidence_literature ; sio:SIO_000772 miriam-pubmed:22592522 ; prov:wasDerivedFrom dgn-void:befree-20150227 ; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^xsd:date . dgn-void:source_evidence_literature a eco:ECO_0000212 ; rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ; rdfs:label "DisGeNET evidence - LITERATURE"@en . } dgn-np:NP1018043.RAiR8ewoWLCvSy96VQiJgV9FcZADKRhbB99obFT4czltw130_publicationInfo { this: dcterms:created "2015-08-25T14:48:11+02:00"^^xsd:dateTime ; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup ; dcterms:subject sio:SIO_000983 ; prv:usedData dgn-void:disgenetv3.0rdf ; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }