@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:NP359883.RAnst5e-wDU56RO6bow-rXiXIs15LaDDg3MpcMMDrl-Po130_head { this: np:hasAssertion dgn-np:NP359883.RAnst5e-wDU56RO6bow-rXiXIs15LaDDg3MpcMMDrl-Po130_assertion; np:hasProvenance dgn-np:NP359883.RAnst5e-wDU56RO6bow-rXiXIs15LaDDg3MpcMMDrl-Po130_provenance; np:hasPublicationInfo dgn-np:NP359883.RAnst5e-wDU56RO6bow-rXiXIs15LaDDg3MpcMMDrl-Po130_publicationInfo; a np:Nanopublication . dgn-np:NP359883.RAnst5e-wDU56RO6bow-rXiXIs15LaDDg3MpcMMDrl-Po130_assertion a np:Assertion . dgn-np:NP359883.RAnst5e-wDU56RO6bow-rXiXIs15LaDDg3MpcMMDrl-Po130_provenance a np:Provenance . dgn-np:NP359883.RAnst5e-wDU56RO6bow-rXiXIs15LaDDg3MpcMMDrl-Po130_publicationInfo a np:PublicationInfo . } dgn-np:NP359883.RAnst5e-wDU56RO6bow-rXiXIs15LaDDg3MpcMMDrl-Po130_assertion { miriam-gene:4914 a ncit:C16612 . lld:C0020074 a ncit:C7057 . dgn-gda:DGN1f50d570febc007371f18ee3e72f2c5c sio:SIO_000628 miriam-gene:4914, lld:C0020074; a sio:SIO_001121 . } dgn-np:NP359883.RAnst5e-wDU56RO6bow-rXiXIs15LaDDg3MpcMMDrl-Po130_provenance { dgn-np:NP359883.RAnst5e-wDU56RO6bow-rXiXIs15LaDDg3MpcMMDrl-Po130_assertion dcterms:description "[Genetics of congenital insensitivity to pain with anhidrosis (CIPA) or hereditary sensory and autonomic neuropathy type IV. Clinical, biological and molecular aspects of mutations in TRKA(NTRK1) gene encoding the receptor tyrosine kinase for nerve growth factor.]. 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:12102460; 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:NP359883.RAnst5e-wDU56RO6bow-rXiXIs15LaDDg3MpcMMDrl-Po130_publicationInfo { this: dcterms:created "2016-05-13T12:44:28+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" . }