http://rdf.disgenet.org/resource/nanopub/NP764643.RAtaPyiqecVOH0nuyYjzg2Pm_tp1oSsyDQfuRSoBne7zY#head http://rdf.disgenet.org/resource/nanopub/NP764643.RAtaPyiqecVOH0nuyYjzg2Pm_tp1oSsyDQfuRSoBne7zY http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP764643.RAtaPyiqecVOH0nuyYjzg2Pm_tp1oSsyDQfuRSoBne7zY#assertion http://rdf.disgenet.org/resource/nanopub/NP764643.RAtaPyiqecVOH0nuyYjzg2Pm_tp1oSsyDQfuRSoBne7zY http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP764643.RAtaPyiqecVOH0nuyYjzg2Pm_tp1oSsyDQfuRSoBne7zY#provenance http://rdf.disgenet.org/resource/nanopub/NP764643.RAtaPyiqecVOH0nuyYjzg2Pm_tp1oSsyDQfuRSoBne7zY http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP764643.RAtaPyiqecVOH0nuyYjzg2Pm_tp1oSsyDQfuRSoBne7zY#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP764643.RAtaPyiqecVOH0nuyYjzg2Pm_tp1oSsyDQfuRSoBne7zY http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP764643.RAtaPyiqecVOH0nuyYjzg2Pm_tp1oSsyDQfuRSoBne7zY#assertion http://rdf.disgenet.org/resource/gda/DGNe9e8ce37bd0d5a1b2f0556c1e5b7caaf http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/4854 http://rdf.disgenet.org/resource/gda/DGNe9e8ce37bd0d5a1b2f0556c1e5b7caaf http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0751587 http://rdf.disgenet.org/resource/gda/DGNe9e8ce37bd0d5a1b2f0556c1e5b7caaf http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP764643.RAtaPyiqecVOH0nuyYjzg2Pm_tp1oSsyDQfuRSoBne7zY#provenance http://rdf.disgenet.org/resource/nanopub/NP764643.RAtaPyiqecVOH0nuyYjzg2Pm_tp1oSsyDQfuRSoBne7zY#assertion http://purl.org/dc/terms/description [The identification of NOTCH3 mutations in patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL) and of TREX1 mutations in retinal vasculopathy with cerebral leukodystrophy (RVCL) have led to new insights on lacunar stroke and small-vessel disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP764643.RAtaPyiqecVOH0nuyYjzg2Pm_tp1oSsyDQfuRSoBne7zY#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/NP764643.RAtaPyiqecVOH0nuyYjzg2Pm_tp1oSsyDQfuRSoBne7zY#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/22113147 http://rdf.disgenet.org/resource/nanopub/NP764643.RAtaPyiqecVOH0nuyYjzg2Pm_tp1oSsyDQfuRSoBne7zY#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP764643.RAtaPyiqecVOH0nuyYjzg2Pm_tp1oSsyDQfuRSoBne7zY#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/NP764643.RAtaPyiqecVOH0nuyYjzg2Pm_tp1oSsyDQfuRSoBne7zY#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP764643.RAtaPyiqecVOH0nuyYjzg2Pm_tp1oSsyDQfuRSoBne7zY http://purl.org/dc/terms/created 2017-10-17T13:15:04+02:00 http://rdf.disgenet.org/resource/nanopub/NP764643.RAtaPyiqecVOH0nuyYjzg2Pm_tp1oSsyDQfuRSoBne7zY http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP764643.RAtaPyiqecVOH0nuyYjzg2Pm_tp1oSsyDQfuRSoBne7zY http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP764643.RAtaPyiqecVOH0nuyYjzg2Pm_tp1oSsyDQfuRSoBne7zY http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP764643.RAtaPyiqecVOH0nuyYjzg2Pm_tp1oSsyDQfuRSoBne7zY http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP764643.RAtaPyiqecVOH0nuyYjzg2Pm_tp1oSsyDQfuRSoBne7zY http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP764643.RAtaPyiqecVOH0nuyYjzg2Pm_tp1oSsyDQfuRSoBne7zY http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP764643.RAtaPyiqecVOH0nuyYjzg2Pm_tp1oSsyDQfuRSoBne7zY http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP764643.RAtaPyiqecVOH0nuyYjzg2Pm_tp1oSsyDQfuRSoBne7zY http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP764643.RAtaPyiqecVOH0nuyYjzg2Pm_tp1oSsyDQfuRSoBne7zY http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP764643.RAtaPyiqecVOH0nuyYjzg2Pm_tp1oSsyDQfuRSoBne7zY http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP764643.RAtaPyiqecVOH0nuyYjzg2Pm_tp1oSsyDQfuRSoBne7zY 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