@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:NP1258673.RASb7wxYBdXu_uKcMnzLqBHfKSf0Hr8N2myJ0_eIltKC4130_head { this: np:hasAssertion dgn-np:NP1258673.RASb7wxYBdXu_uKcMnzLqBHfKSf0Hr8N2myJ0_eIltKC4130_assertion; np:hasProvenance dgn-np:NP1258673.RASb7wxYBdXu_uKcMnzLqBHfKSf0Hr8N2myJ0_eIltKC4130_provenance; np:hasPublicationInfo dgn-np:NP1258673.RASb7wxYBdXu_uKcMnzLqBHfKSf0Hr8N2myJ0_eIltKC4130_publicationInfo; a np:Nanopublication . dgn-np:NP1258673.RASb7wxYBdXu_uKcMnzLqBHfKSf0Hr8N2myJ0_eIltKC4130_assertion a np:Assertion . dgn-np:NP1258673.RASb7wxYBdXu_uKcMnzLqBHfKSf0Hr8N2myJ0_eIltKC4130_provenance a np:Provenance . dgn-np:NP1258673.RASb7wxYBdXu_uKcMnzLqBHfKSf0Hr8N2myJ0_eIltKC4130_publicationInfo a np:PublicationInfo . } dgn-np:NP1258673.RASb7wxYBdXu_uKcMnzLqBHfKSf0Hr8N2myJ0_eIltKC4130_assertion { miriam-gene:5621 a ncit:C16612 . lld:C0442874 a ncit:C7057 . dgn-gda:DGNc18453ac2e32fd11dcc6f3fd56c794bd sio:SIO_000628 miriam-gene:5621, lld:C0442874; a sio:SIO_001121 . } dgn-np:NP1258673.RASb7wxYBdXu_uKcMnzLqBHfKSf0Hr8N2myJ0_eIltKC4130_provenance { dgn-np:NP1258673.RASb7wxYBdXu_uKcMnzLqBHfKSf0Hr8N2myJ0_eIltKC4130_assertion dcterms:description "[Although the potential transmissibility of this new prion disease is probably extremely low, we advocate PrP gene analysis before biopsy in the investigation of peripheral and autonomic neuropathies, or for patients with unexplained diarrhoea and neuropathy.]. 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:25623792; 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:NP1258673.RASb7wxYBdXu_uKcMnzLqBHfKSf0Hr8N2myJ0_eIltKC4130_publicationInfo { this: dcterms:created "2016-05-13T12:51:16+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" . }