@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:NP125213.RA3JkR9XVz_ypN2QoY0pmT0FbqpF31MwRVfa8einS034Y130_head { this: np:hasAssertion dgn-np:NP125213.RA3JkR9XVz_ypN2QoY0pmT0FbqpF31MwRVfa8einS034Y130_assertion; np:hasProvenance dgn-np:NP125213.RA3JkR9XVz_ypN2QoY0pmT0FbqpF31MwRVfa8einS034Y130_provenance; np:hasPublicationInfo dgn-np:NP125213.RA3JkR9XVz_ypN2QoY0pmT0FbqpF31MwRVfa8einS034Y130_publicationInfo; a np:Nanopublication . dgn-np:NP125213.RA3JkR9XVz_ypN2QoY0pmT0FbqpF31MwRVfa8einS034Y130_assertion a np:Assertion . dgn-np:NP125213.RA3JkR9XVz_ypN2QoY0pmT0FbqpF31MwRVfa8einS034Y130_provenance a np:Provenance . dgn-np:NP125213.RA3JkR9XVz_ypN2QoY0pmT0FbqpF31MwRVfa8einS034Y130_publicationInfo a np:PublicationInfo . } dgn-np:NP125213.RA3JkR9XVz_ypN2QoY0pmT0FbqpF31MwRVfa8einS034Y130_assertion { miriam-gene:6392 a ncit:C16612 . lld:C0001624 a ncit:C7057 . dgn-gda:DGN76467bc7b85dd8422fb59b1682f2c476 sio:SIO_000628 miriam-gene:6392, lld:C0001624; a sio:SIO_001122 . } dgn-np:NP125213.RA3JkR9XVz_ypN2QoY0pmT0FbqpF31MwRVfa8einS034Y130_provenance { dgn-np:NP125213.RA3JkR9XVz_ypN2QoY0pmT0FbqpF31MwRVfa8einS034Y130_assertion dcterms:description "[The results of our study show that genetic predisposition is frequent in chromaffin tissue tumours, which indicates that DNA analysis is necessary in every case, also because of possible atypical clinical presentation. (Pol J Endocrinol 2010; 61 (1): 43-4]. 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:20205103; prov:wasDerivedFrom dgn-void:gad-20150221; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP125213.RA3JkR9XVz_ypN2QoY0pmT0FbqpF31MwRVfa8einS034Y130_publicationInfo { this: dcterms:created "2015-08-25T14:38:50+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" . }