@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:NP1183459.RAfD-qTmW1MPuqguhtUf7b2Lerul7VUMs987OpjNRfcnU130_head { this: np:hasAssertion dgn-np:NP1183459.RAfD-qTmW1MPuqguhtUf7b2Lerul7VUMs987OpjNRfcnU130_assertion; np:hasProvenance dgn-np:NP1183459.RAfD-qTmW1MPuqguhtUf7b2Lerul7VUMs987OpjNRfcnU130_provenance; np:hasPublicationInfo dgn-np:NP1183459.RAfD-qTmW1MPuqguhtUf7b2Lerul7VUMs987OpjNRfcnU130_publicationInfo; a np:Nanopublication . dgn-np:NP1183459.RAfD-qTmW1MPuqguhtUf7b2Lerul7VUMs987OpjNRfcnU130_assertion a np:Assertion . dgn-np:NP1183459.RAfD-qTmW1MPuqguhtUf7b2Lerul7VUMs987OpjNRfcnU130_provenance a np:Provenance . dgn-np:NP1183459.RAfD-qTmW1MPuqguhtUf7b2Lerul7VUMs987OpjNRfcnU130_publicationInfo a np:PublicationInfo . } dgn-np:NP1183459.RAfD-qTmW1MPuqguhtUf7b2Lerul7VUMs987OpjNRfcnU130_assertion { miriam-gene:257641 a ncit:C16612 . lld:C0235031 a ncit:C7057 . dgn-gda:DGNf450bc32d2a6a7e4b9ce0e0ff859df36 sio:SIO_000628 miriam-gene:257641, lld:C0235031; a sio:SIO_001121 . } dgn-np:NP1183459.RAfD-qTmW1MPuqguhtUf7b2Lerul7VUMs987OpjNRfcnU130_provenance { dgn-np:NP1183459.RAfD-qTmW1MPuqguhtUf7b2Lerul7VUMs987OpjNRfcnU130_assertion dcterms:description "[Auditory testing revealed a progressive high-frequency hearing loss in Npc1 (-/-) mice that is present as early as postnatal day 20 (P20), well before the onset of overt neurological symptoms, with evidence of abnormalities involving the cochlea, auditory nerve, and brainstem auditory centers.]. 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:24839095; 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:NP1183459.RAfD-qTmW1MPuqguhtUf7b2Lerul7VUMs987OpjNRfcnU130_publicationInfo { this: dcterms:created "2016-05-13T12:50:42+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" . }