@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:NP419988.RAePCsb0ujKhxeZvHJ8ALozeQDPNfPVP3_Geqhnvp6hOc130_head { this: np:hasAssertion dgn-np:NP419988.RAePCsb0ujKhxeZvHJ8ALozeQDPNfPVP3_Geqhnvp6hOc130_assertion; np:hasProvenance dgn-np:NP419988.RAePCsb0ujKhxeZvHJ8ALozeQDPNfPVP3_Geqhnvp6hOc130_provenance; np:hasPublicationInfo dgn-np:NP419988.RAePCsb0ujKhxeZvHJ8ALozeQDPNfPVP3_Geqhnvp6hOc130_publicationInfo; a np:Nanopublication . dgn-np:NP419988.RAePCsb0ujKhxeZvHJ8ALozeQDPNfPVP3_Geqhnvp6hOc130_assertion a np:Assertion . dgn-np:NP419988.RAePCsb0ujKhxeZvHJ8ALozeQDPNfPVP3_Geqhnvp6hOc130_provenance a np:Provenance . dgn-np:NP419988.RAePCsb0ujKhxeZvHJ8ALozeQDPNfPVP3_Geqhnvp6hOc130_publicationInfo a np:PublicationInfo . } dgn-np:NP419988.RAePCsb0ujKhxeZvHJ8ALozeQDPNfPVP3_Geqhnvp6hOc130_assertion { miriam-gene:2632 a ncit:C16612 . lld:C1849722 a ncit:C7057 . dgn-gda:DGNde9ac27a2801e2de767b2577065abf66 sio:SIO_000628 miriam-gene:2632, lld:C1849722; a sio:SIO_001121 . } dgn-np:NP419988.RAePCsb0ujKhxeZvHJ8ALozeQDPNfPVP3_Geqhnvp6hOc130_provenance { dgn-np:NP419988.RAePCsb0ujKhxeZvHJ8ALozeQDPNfPVP3_Geqhnvp6hOc130_assertion dcterms:description "[Our findings widen the spectrum of APBD genotypes, underline the importance of performing GBE analysis in all APBD patients, and suggest that brain white matter degeneration in APBD may result from tissue damage involving axons and myelin.]. 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:17994551; 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:NP419988.RAePCsb0ujKhxeZvHJ8ALozeQDPNfPVP3_Geqhnvp6hOc130_publicationInfo { this: dcterms:created "2015-08-25T14:41:44+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" . }