@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:NP907237.RAl0_SGYIDPCOGZHjN6ZizIO-HBqAxvJUb1CjvV5EMI98130_head { this: np:hasAssertion dgn-np:NP907237.RAl0_SGYIDPCOGZHjN6ZizIO-HBqAxvJUb1CjvV5EMI98130_assertion; np:hasProvenance dgn-np:NP907237.RAl0_SGYIDPCOGZHjN6ZizIO-HBqAxvJUb1CjvV5EMI98130_provenance; np:hasPublicationInfo dgn-np:NP907237.RAl0_SGYIDPCOGZHjN6ZizIO-HBqAxvJUb1CjvV5EMI98130_publicationInfo; a np:Nanopublication . dgn-np:NP907237.RAl0_SGYIDPCOGZHjN6ZizIO-HBqAxvJUb1CjvV5EMI98130_assertion a np:Assertion . dgn-np:NP907237.RAl0_SGYIDPCOGZHjN6ZizIO-HBqAxvJUb1CjvV5EMI98130_provenance a np:Provenance . dgn-np:NP907237.RAl0_SGYIDPCOGZHjN6ZizIO-HBqAxvJUb1CjvV5EMI98130_publicationInfo a np:PublicationInfo . } dgn-np:NP907237.RAl0_SGYIDPCOGZHjN6ZizIO-HBqAxvJUb1CjvV5EMI98130_assertion { miriam-gene:4653 a ncit:C16612 . lld:C0017601 a ncit:C7057 . dgn-gda:DGNa2e34cc363ac81656f7e0ac91baa9422 sio:SIO_000628 miriam-gene:4653, lld:C0017601; a sio:SIO_001121 . } dgn-np:NP907237.RAl0_SGYIDPCOGZHjN6ZizIO-HBqAxvJUb1CjvV5EMI98130_provenance { dgn-np:NP907237.RAl0_SGYIDPCOGZHjN6ZizIO-HBqAxvJUb1CjvV5EMI98130_assertion dcterms:description "[The most common identifiable cause of primary juvenile open-angle glaucoma across most populations remains heterozygous (autosomal dominant) MYOC mutation, underlying up to one-third of cases and possibly sometimes involved in earlier and later onset glaucomas Although primary adult-onset open-angle glaucoma usually does not follow simple Mendelian genetics and is etiologically complex, genome-wide association studies are uncovering genetic susceptibility factors.]. 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:21730848; prov:wasDerivedFrom dgn-void:befree-2016; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP907237.RAl0_SGYIDPCOGZHjN6ZizIO-HBqAxvJUb1CjvV5EMI98130_publicationInfo { this: dcterms:created "2016-05-13T12:48:35+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 "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }