@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:NP335289.RAc44CbTzUkr2BVTDYgxR3tJI8rBoJKlg445XfZW0EzKo130_head { this: np:hasAssertion dgn-np:NP335289.RAc44CbTzUkr2BVTDYgxR3tJI8rBoJKlg445XfZW0EzKo130_assertion; np:hasProvenance dgn-np:NP335289.RAc44CbTzUkr2BVTDYgxR3tJI8rBoJKlg445XfZW0EzKo130_provenance; np:hasPublicationInfo dgn-np:NP335289.RAc44CbTzUkr2BVTDYgxR3tJI8rBoJKlg445XfZW0EzKo130_publicationInfo; a np:Nanopublication . dgn-np:NP335289.RAc44CbTzUkr2BVTDYgxR3tJI8rBoJKlg445XfZW0EzKo130_assertion a np:Assertion . dgn-np:NP335289.RAc44CbTzUkr2BVTDYgxR3tJI8rBoJKlg445XfZW0EzKo130_provenance a np:Provenance . dgn-np:NP335289.RAc44CbTzUkr2BVTDYgxR3tJI8rBoJKlg445XfZW0EzKo130_publicationInfo a np:PublicationInfo . } dgn-np:NP335289.RAc44CbTzUkr2BVTDYgxR3tJI8rBoJKlg445XfZW0EzKo130_assertion { miriam-gene:1493 a ncit:C16612 . lld:C0018213 a ncit:C7057 . dgn-gda:DGN762abf296aeeb509d95163ebfb3cf438 sio:SIO_000628 miriam-gene:1493, lld:C0018213; a sio:SIO_001121 . } dgn-np:NP335289.RAc44CbTzUkr2BVTDYgxR3tJI8rBoJKlg445XfZW0EzKo130_provenance { dgn-np:NP335289.RAc44CbTzUkr2BVTDYgxR3tJI8rBoJKlg445XfZW0EzKo130_assertion dcterms:description "[Previous data from our laboratory and others have suggested that GO has no specific genetic component distinct from GD itself, while other reports have occasionally appeared suggesting that polymorphisms in genes such as CTLA4 and IL23R specifically increase the risk for GO.]. 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:22663548; 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:NP335289.RAc44CbTzUkr2BVTDYgxR3tJI8rBoJKlg445XfZW0EzKo130_publicationInfo { this: dcterms:created "2015-08-25T14:40:53+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" . }