@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:NP1095473.RAgMLbyE7sZJThFEAnVz9K_G7I45nlcLH9rI77ZF0N0rY130_head { this: np:hasAssertion dgn-np:NP1095473.RAgMLbyE7sZJThFEAnVz9K_G7I45nlcLH9rI77ZF0N0rY130_assertion; np:hasProvenance dgn-np:NP1095473.RAgMLbyE7sZJThFEAnVz9K_G7I45nlcLH9rI77ZF0N0rY130_provenance; np:hasPublicationInfo dgn-np:NP1095473.RAgMLbyE7sZJThFEAnVz9K_G7I45nlcLH9rI77ZF0N0rY130_publicationInfo; a np:Nanopublication . dgn-np:NP1095473.RAgMLbyE7sZJThFEAnVz9K_G7I45nlcLH9rI77ZF0N0rY130_assertion a np:Assertion . dgn-np:NP1095473.RAgMLbyE7sZJThFEAnVz9K_G7I45nlcLH9rI77ZF0N0rY130_provenance a np:Provenance . dgn-np:NP1095473.RAgMLbyE7sZJThFEAnVz9K_G7I45nlcLH9rI77ZF0N0rY130_publicationInfo a np:PublicationInfo . } dgn-np:NP1095473.RAgMLbyE7sZJThFEAnVz9K_G7I45nlcLH9rI77ZF0N0rY130_assertion { miriam-gene:8929 a ncit:C16612 . lld:C0027819 a ncit:C7057 . dgn-gda:DGN062b77815dd604701c575a06c57bc9d6 sio:SIO_000628 miriam-gene:8929, lld:C0027819; a sio:SIO_001121 . } dgn-np:NP1095473.RAgMLbyE7sZJThFEAnVz9K_G7I45nlcLH9rI77ZF0N0rY130_provenance { dgn-np:NP1095473.RAgMLbyE7sZJThFEAnVz9K_G7I45nlcLH9rI77ZF0N0rY130_assertion dcterms:description "[Our results suggest that certain PHOX2B variants associated with neuroblastoma pathogenesis, because of their inability to bind to key interacting proteins such as HPCAL1, may predispose to this malignancy by impeding the differentiation of immature sympathetic neurons.]. 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:23873030; 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:NP1095473.RAgMLbyE7sZJThFEAnVz9K_G7I45nlcLH9rI77ZF0N0rY130_publicationInfo { this: dcterms:created "2016-05-13T12:50:02+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" . }