@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:NP1365919.RAokqpZeolSQHyVLvfq6uDueLBrNk-xwn3s1DYSKroi0E130_head { this: np:hasAssertion dgn-np:NP1365919.RAokqpZeolSQHyVLvfq6uDueLBrNk-xwn3s1DYSKroi0E130_assertion; np:hasProvenance dgn-np:NP1365919.RAokqpZeolSQHyVLvfq6uDueLBrNk-xwn3s1DYSKroi0E130_provenance; np:hasPublicationInfo dgn-np:NP1365919.RAokqpZeolSQHyVLvfq6uDueLBrNk-xwn3s1DYSKroi0E130_publicationInfo; a np:Nanopublication . dgn-np:NP1365919.RAokqpZeolSQHyVLvfq6uDueLBrNk-xwn3s1DYSKroi0E130_assertion a np:Assertion . dgn-np:NP1365919.RAokqpZeolSQHyVLvfq6uDueLBrNk-xwn3s1DYSKroi0E130_provenance a np:Provenance . dgn-np:NP1365919.RAokqpZeolSQHyVLvfq6uDueLBrNk-xwn3s1DYSKroi0E130_publicationInfo a np:PublicationInfo . } dgn-np:NP1365919.RAokqpZeolSQHyVLvfq6uDueLBrNk-xwn3s1DYSKroi0E130_assertion { miriam-gene:4647 a ncit:C16612 . lld:C1568247 a ncit:C7057 . dgn-gda:DGNe2826ef0919ec08d275fc39ce24c7694 sio:SIO_000628 miriam-gene:4647, lld:C1568247; a sio:SIO_001121 . } dgn-np:NP1365919.RAokqpZeolSQHyVLvfq6uDueLBrNk-xwn3s1DYSKroi0E130_provenance { dgn-np:NP1365919.RAokqpZeolSQHyVLvfq6uDueLBrNk-xwn3s1DYSKroi0E130_assertion dcterms:description "[Primers covering the complete myosin VIIA coding sequence as well as the 3' non coding sequence were designed, allowing direct sequence analysis of each of the 48 coding exons and flanking splice sites in seven patients affected by USH1.]. 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:9002678; 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:NP1365919.RAokqpZeolSQHyVLvfq6uDueLBrNk-xwn3s1DYSKroi0E130_publicationInfo { this: dcterms:created "2016-05-13T12:52:05+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" . }