@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:NP438703.RAl_4sylFo4_--N0NJ7CL0-G61PKrqXceF_aUMwZBHYNw130_head { this: np:hasAssertion dgn-np:NP438703.RAl_4sylFo4_--N0NJ7CL0-G61PKrqXceF_aUMwZBHYNw130_assertion; np:hasProvenance dgn-np:NP438703.RAl_4sylFo4_--N0NJ7CL0-G61PKrqXceF_aUMwZBHYNw130_provenance; np:hasPublicationInfo dgn-np:NP438703.RAl_4sylFo4_--N0NJ7CL0-G61PKrqXceF_aUMwZBHYNw130_publicationInfo; a np:Nanopublication . dgn-np:NP438703.RAl_4sylFo4_--N0NJ7CL0-G61PKrqXceF_aUMwZBHYNw130_assertion a np:Assertion . dgn-np:NP438703.RAl_4sylFo4_--N0NJ7CL0-G61PKrqXceF_aUMwZBHYNw130_provenance a np:Provenance . dgn-np:NP438703.RAl_4sylFo4_--N0NJ7CL0-G61PKrqXceF_aUMwZBHYNw130_publicationInfo a np:PublicationInfo . } dgn-np:NP438703.RAl_4sylFo4_--N0NJ7CL0-G61PKrqXceF_aUMwZBHYNw130_assertion { miriam-gene:4854 a ncit:C16612 . lld:C0042373 a ncit:C7057 . dgn-gda:DGNfa7a47f70cdd68aeeabbc06fc9316b44 sio:SIO_000628 miriam-gene:4854, lld:C0042373; a sio:SIO_001121 . } dgn-np:NP438703.RAl_4sylFo4_--N0NJ7CL0-G61PKrqXceF_aUMwZBHYNw130_provenance { dgn-np:NP438703.RAl_4sylFo4_--N0NJ7CL0-G61PKrqXceF_aUMwZBHYNw130_assertion dcterms:description "[Therefore, we propose to consider a replacement for the name CADASIL that better reflects the morphological picture of the disease like, for example, cerebral autosomal dominant vasculopathy with subcortical infarcts and leukoencephalopathy (CADVaSIL) or, to preserve the commonly known acronym, cerebral autosomal dominant angiopathy with subcortical infarcts and leukoencephalopathy.]. 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:15068168; 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:NP438703.RAl_4sylFo4_--N0NJ7CL0-G61PKrqXceF_aUMwZBHYNw130_publicationInfo { this: dcterms:created "2016-05-13T12:45:04+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" . }