@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:NP662874.RASu_LDVSdISQplyMvTzyD67rrNmCKJsqqwCH6rH2oapI130_head { this: np:hasAssertion dgn-np:NP662874.RASu_LDVSdISQplyMvTzyD67rrNmCKJsqqwCH6rH2oapI130_assertion; np:hasProvenance dgn-np:NP662874.RASu_LDVSdISQplyMvTzyD67rrNmCKJsqqwCH6rH2oapI130_provenance; np:hasPublicationInfo dgn-np:NP662874.RASu_LDVSdISQplyMvTzyD67rrNmCKJsqqwCH6rH2oapI130_publicationInfo; a np:Nanopublication . dgn-np:NP662874.RASu_LDVSdISQplyMvTzyD67rrNmCKJsqqwCH6rH2oapI130_assertion a np:Assertion . dgn-np:NP662874.RASu_LDVSdISQplyMvTzyD67rrNmCKJsqqwCH6rH2oapI130_provenance a np:Provenance . dgn-np:NP662874.RASu_LDVSdISQplyMvTzyD67rrNmCKJsqqwCH6rH2oapI130_publicationInfo a np:PublicationInfo . } dgn-np:NP662874.RASu_LDVSdISQplyMvTzyD67rrNmCKJsqqwCH6rH2oapI130_assertion { miriam-gene:5873 a ncit:C16612 . lld:C1876214 a ncit:C7057 . dgn-gda:DGN380d916f6347bea5f0a8b6b5027aeb64 sio:SIO_000628 miriam-gene:5873, lld:C1876214; a sio:SIO_001121 . } dgn-np:NP662874.RASu_LDVSdISQplyMvTzyD67rrNmCKJsqqwCH6rH2oapI130_provenance { dgn-np:NP662874.RASu_LDVSdISQplyMvTzyD67rrNmCKJsqqwCH6rH2oapI130_assertion dcterms:description "[Rab27a plays a pivotal role in the transport of melanosomes to dendrite tips of melanocytes and mutations in RAB27A, which impair melanosome transport cause the pigmentary dilution and the immune deficiency found in several patients with Griscelli syndrome (GS).]. 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:12531900; 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:NP662874.RASu_LDVSdISQplyMvTzyD67rrNmCKJsqqwCH6rH2oapI130_publicationInfo { this: dcterms:created "2015-08-25T14:44:18+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" . }