@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:NP975291.RAzCL_mkIEgPQOEG2fPirzGOtfMrJLayysHzSPBisJF1g130_head { this: np:hasAssertion dgn-np:NP975291.RAzCL_mkIEgPQOEG2fPirzGOtfMrJLayysHzSPBisJF1g130_assertion; np:hasProvenance dgn-np:NP975291.RAzCL_mkIEgPQOEG2fPirzGOtfMrJLayysHzSPBisJF1g130_provenance; np:hasPublicationInfo dgn-np:NP975291.RAzCL_mkIEgPQOEG2fPirzGOtfMrJLayysHzSPBisJF1g130_publicationInfo; a np:Nanopublication . dgn-np:NP975291.RAzCL_mkIEgPQOEG2fPirzGOtfMrJLayysHzSPBisJF1g130_assertion a np:Assertion . dgn-np:NP975291.RAzCL_mkIEgPQOEG2fPirzGOtfMrJLayysHzSPBisJF1g130_provenance a np:Provenance . dgn-np:NP975291.RAzCL_mkIEgPQOEG2fPirzGOtfMrJLayysHzSPBisJF1g130_publicationInfo a np:PublicationInfo . } dgn-np:NP975291.RAzCL_mkIEgPQOEG2fPirzGOtfMrJLayysHzSPBisJF1g130_assertion { miriam-gene:149233 a ncit:C16612 . lld:C0018213 a ncit:C7057 . dgn-gda:DGNacb3634653bd679fbad805776845c1e7 sio:SIO_000628 miriam-gene:149233, lld:C0018213; a sio:SIO_001121 . } dgn-np:NP975291.RAzCL_mkIEgPQOEG2fPirzGOtfMrJLayysHzSPBisJF1g130_provenance { dgn-np:NP975291.RAzCL_mkIEgPQOEG2fPirzGOtfMrJLayysHzSPBisJF1g130_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:NP975291.RAzCL_mkIEgPQOEG2fPirzGOtfMrJLayysHzSPBisJF1g130_publicationInfo { this: dcterms:created "2015-08-25T14:47:35+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" . }