@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:NP107158.RArcWA4ihLe-Sl_c1xKOpbOPB5A2uur11LiyXr_fKgFiE130_head { this: np:hasAssertion dgn-np:NP107158.RArcWA4ihLe-Sl_c1xKOpbOPB5A2uur11LiyXr_fKgFiE130_assertion; np:hasProvenance dgn-np:NP107158.RArcWA4ihLe-Sl_c1xKOpbOPB5A2uur11LiyXr_fKgFiE130_provenance; np:hasPublicationInfo dgn-np:NP107158.RArcWA4ihLe-Sl_c1xKOpbOPB5A2uur11LiyXr_fKgFiE130_publicationInfo; a np:Nanopublication . dgn-np:NP107158.RArcWA4ihLe-Sl_c1xKOpbOPB5A2uur11LiyXr_fKgFiE130_assertion a np:Assertion . dgn-np:NP107158.RArcWA4ihLe-Sl_c1xKOpbOPB5A2uur11LiyXr_fKgFiE130_provenance a np:Provenance . dgn-np:NP107158.RArcWA4ihLe-Sl_c1xKOpbOPB5A2uur11LiyXr_fKgFiE130_publicationInfo a np:PublicationInfo . } dgn-np:NP107158.RArcWA4ihLe-Sl_c1xKOpbOPB5A2uur11LiyXr_fKgFiE130_assertion { miriam-gene:2296 a ncit:C16612 . lld:C0017601 a ncit:C7057 . dgn-gda:DGN1b3cef56924fee247013c70aa7f013ad sio:SIO_000628 miriam-gene:2296, lld:C0017601; a sio:SIO_001122 . } dgn-np:NP107158.RArcWA4ihLe-Sl_c1xKOpbOPB5A2uur11LiyXr_fKgFiE130_provenance { dgn-np:NP107158.RArcWA4ihLe-Sl_c1xKOpbOPB5A2uur11LiyXr_fKgFiE130_assertion dcterms:description "[MYOC and FOXC1 mutations are not involved in pathogenesis of primary congenital glaucoma in our patients. Thus, it is important to screen other loci for involvement in congenital glaucoma in cases which are negative or heterozygous for CYP1B1 mutations to]. 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:21031026; prov:wasDerivedFrom dgn-void:gad-20150221; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP107158.RArcWA4ihLe-Sl_c1xKOpbOPB5A2uur11LiyXr_fKgFiE130_publicationInfo { this: dcterms:created "2015-08-25T14:38:39+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" . }