http://rdf.disgenet.org/resource/nanopub/NP764743.RAaodc6HBo6vW2814K75ixnbG5sjIr8g_oaLdnf61gNUA#head
http://rdf.disgenet.org/resource/nanopub/NP764743.RAaodc6HBo6vW2814K75ixnbG5sjIr8g_oaLdnf61gNUA
http://www.nanopub.org/nschema#hasAssertion
http://rdf.disgenet.org/resource/nanopub/NP764743.RAaodc6HBo6vW2814K75ixnbG5sjIr8g_oaLdnf61gNUA#assertion
http://rdf.disgenet.org/resource/nanopub/NP764743.RAaodc6HBo6vW2814K75ixnbG5sjIr8g_oaLdnf61gNUA
http://www.nanopub.org/nschema#hasProvenance
http://rdf.disgenet.org/resource/nanopub/NP764743.RAaodc6HBo6vW2814K75ixnbG5sjIr8g_oaLdnf61gNUA#provenance
http://rdf.disgenet.org/resource/nanopub/NP764743.RAaodc6HBo6vW2814K75ixnbG5sjIr8g_oaLdnf61gNUA
http://www.nanopub.org/nschema#hasPublicationInfo
http://rdf.disgenet.org/resource/nanopub/NP764743.RAaodc6HBo6vW2814K75ixnbG5sjIr8g_oaLdnf61gNUA#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP764743.RAaodc6HBo6vW2814K75ixnbG5sjIr8g_oaLdnf61gNUA
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://www.nanopub.org/nschema#Nanopublication
http://rdf.disgenet.org/resource/nanopub/NP764743.RAaodc6HBo6vW2814K75ixnbG5sjIr8g_oaLdnf61gNUA#assertion
http://rdf.disgenet.org/resource/gda/DGN7652dd5edb6bdcbf6e4a0ae5ef6aefe6
http://semanticscience.org/resource/SIO_000628
http://identifiers.org/ncbigene/4854
http://rdf.disgenet.org/resource/gda/DGN7652dd5edb6bdcbf6e4a0ae5ef6aefe6
http://semanticscience.org/resource/SIO_000628
http://linkedlifedata.com/resource/umls/id/C0751587
http://rdf.disgenet.org/resource/gda/DGN7652dd5edb6bdcbf6e4a0ae5ef6aefe6
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://semanticscience.org/resource/SIO_001121
http://rdf.disgenet.org/resource/nanopub/NP764743.RAaodc6HBo6vW2814K75ixnbG5sjIr8g_oaLdnf61gNUA#provenance
http://rdf.disgenet.org/resource/nanopub/NP764743.RAaodc6HBo6vW2814K75ixnbG5sjIr8g_oaLdnf61gNUA#assertion
http://purl.org/dc/terms/description
[The most common form of familial vascular dementia is considered to be CADASIL or cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, which is now also increasingly manifest in the United Kingdom.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
http://rdf.disgenet.org/resource/nanopub/NP764743.RAaodc6HBo6vW2814K75ixnbG5sjIr8g_oaLdnf61gNUA#assertion
http://purl.org/ontology/wi/core#evidence
http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature
http://rdf.disgenet.org/resource/nanopub/NP764743.RAaodc6HBo6vW2814K75ixnbG5sjIr8g_oaLdnf61gNUA#assertion
http://semanticscience.org/resource/SIO_000772
http://identifiers.org/pubmed/10818518
http://rdf.disgenet.org/resource/nanopub/NP764743.RAaodc6HBo6vW2814K75ixnbG5sjIr8g_oaLdnf61gNUA#assertion
http://www.w3.org/ns/prov#wasDerivedFrom
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://rdf.disgenet.org/resource/nanopub/NP764743.RAaodc6HBo6vW2814K75ixnbG5sjIr8g_oaLdnf61gNUA#assertion
http://www.w3.org/ns/prov#wasGeneratedBy
http://purl.obolibrary.org/obo/ECO_0000203
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://purl.org/pav/importedOn
2017-02-19
http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.obolibrary.org/obo/ECO_0000212
http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature
http://www.w3.org/2000/01/rdf-schema#comment
Gene-disease associations inferred from text-mining the literature.
http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature
http://www.w3.org/2000/01/rdf-schema#label
DisGeNET evidence - LITERATURE
http://rdf.disgenet.org/resource/nanopub/NP764743.RAaodc6HBo6vW2814K75ixnbG5sjIr8g_oaLdnf61gNUA#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP764743.RAaodc6HBo6vW2814K75ixnbG5sjIr8g_oaLdnf61gNUA
http://purl.org/dc/terms/created
2017-10-17T13:15:04+02:00
http://rdf.disgenet.org/resource/nanopub/NP764743.RAaodc6HBo6vW2814K75ixnbG5sjIr8g_oaLdnf61gNUA
http://purl.org/dc/terms/rights
http://opendatacommons.org/licenses/odbl/1.0/
http://rdf.disgenet.org/resource/nanopub/NP764743.RAaodc6HBo6vW2814K75ixnbG5sjIr8g_oaLdnf61gNUA
http://purl.org/dc/terms/rightsHolder
http://rdf.disgenet.org/v5.0.0/void/IBIGroup
http://rdf.disgenet.org/resource/nanopub/NP764743.RAaodc6HBo6vW2814K75ixnbG5sjIr8g_oaLdnf61gNUA
http://purl.org/dc/terms/subject
http://semanticscience.org/resource/SIO_000983
http://rdf.disgenet.org/resource/nanopub/NP764743.RAaodc6HBo6vW2814K75ixnbG5sjIr8g_oaLdnf61gNUA
http://purl.org/net/provenance/ns#usedData
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://rdf.disgenet.org/resource/nanopub/NP764743.RAaodc6HBo6vW2814K75ixnbG5sjIr8g_oaLdnf61gNUA
http://purl.org/pav/authoredBy
http://orcid.org/0000-0001-5999-6269
http://rdf.disgenet.org/resource/nanopub/NP764743.RAaodc6HBo6vW2814K75ixnbG5sjIr8g_oaLdnf61gNUA
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-7534-7661
http://rdf.disgenet.org/resource/nanopub/NP764743.RAaodc6HBo6vW2814K75ixnbG5sjIr8g_oaLdnf61gNUA
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-9383-528X
http://rdf.disgenet.org/resource/nanopub/NP764743.RAaodc6HBo6vW2814K75ixnbG5sjIr8g_oaLdnf61gNUA
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP764743.RAaodc6HBo6vW2814K75ixnbG5sjIr8g_oaLdnf61gNUA
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-1244-7654
http://rdf.disgenet.org/resource/nanopub/NP764743.RAaodc6HBo6vW2814K75ixnbG5sjIr8g_oaLdnf61gNUA
http://purl.org/pav/createdBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP764743.RAaodc6HBo6vW2814K75ixnbG5sjIr8g_oaLdnf61gNUA
http://purl.org/pav/version
v5.0.0.0
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://purl.org/pav/version
v5.0.0