@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:NP612804.RAjh1H2MH_IYe-PWRes1woMpGYowmal4P5n9lw_h-O3-U130_head { this: np:hasAssertion dgn-np:NP612804.RAjh1H2MH_IYe-PWRes1woMpGYowmal4P5n9lw_h-O3-U130_assertion; np:hasProvenance dgn-np:NP612804.RAjh1H2MH_IYe-PWRes1woMpGYowmal4P5n9lw_h-O3-U130_provenance; np:hasPublicationInfo dgn-np:NP612804.RAjh1H2MH_IYe-PWRes1woMpGYowmal4P5n9lw_h-O3-U130_publicationInfo; a np:Nanopublication . dgn-np:NP612804.RAjh1H2MH_IYe-PWRes1woMpGYowmal4P5n9lw_h-O3-U130_assertion a np:Assertion . dgn-np:NP612804.RAjh1H2MH_IYe-PWRes1woMpGYowmal4P5n9lw_h-O3-U130_provenance a np:Provenance . dgn-np:NP612804.RAjh1H2MH_IYe-PWRes1woMpGYowmal4P5n9lw_h-O3-U130_publicationInfo a np:PublicationInfo . } dgn-np:NP612804.RAjh1H2MH_IYe-PWRes1woMpGYowmal4P5n9lw_h-O3-U130_assertion { miriam-gene:5132 a ncit:C16612 . lld:C1568249 a ncit:C7057 . dgn-gda:DGN796e2248402e4cfda2be899ef1dda075 sio:SIO_000628 miriam-gene:5132, lld:C1568249; a sio:SIO_001121 . } dgn-np:NP612804.RAjh1H2MH_IYe-PWRes1woMpGYowmal4P5n9lw_h-O3-U130_provenance { dgn-np:NP612804.RAjh1H2MH_IYe-PWRes1woMpGYowmal4P5n9lw_h-O3-U130_assertion dcterms:description "[In conclusion, the phosducin gene did not show mutations consistent with it being the causative gene for USH2, but its possible pathogenicity in AZOOR or other retinopathies remains an open question which may be answered by further analysis.]. 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:8740692; 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:NP612804.RAjh1H2MH_IYe-PWRes1woMpGYowmal4P5n9lw_h-O3-U130_publicationInfo { this: dcterms:created "2015-08-25T14:43:46+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" . }