http://rdf.disgenet.org/resource/nanopub/NP1116827.RAxxFxTFylKfNYCbYpIBFiHmB_FtGBE-cjxk8TufN2HnM#head http://rdf.disgenet.org/resource/nanopub/NP1116827.RAxxFxTFylKfNYCbYpIBFiHmB_FtGBE-cjxk8TufN2HnM http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP1116827.RAxxFxTFylKfNYCbYpIBFiHmB_FtGBE-cjxk8TufN2HnM#assertion http://rdf.disgenet.org/resource/nanopub/NP1116827.RAxxFxTFylKfNYCbYpIBFiHmB_FtGBE-cjxk8TufN2HnM http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP1116827.RAxxFxTFylKfNYCbYpIBFiHmB_FtGBE-cjxk8TufN2HnM#provenance http://rdf.disgenet.org/resource/nanopub/NP1116827.RAxxFxTFylKfNYCbYpIBFiHmB_FtGBE-cjxk8TufN2HnM http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP1116827.RAxxFxTFylKfNYCbYpIBFiHmB_FtGBE-cjxk8TufN2HnM#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP1116827.RAxxFxTFylKfNYCbYpIBFiHmB_FtGBE-cjxk8TufN2HnM http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP1116827.RAxxFxTFylKfNYCbYpIBFiHmB_FtGBE-cjxk8TufN2HnM#assertion http://rdf.disgenet.org/resource/gda/DGNf925e88b432af4c2c3fb5ab7c1a015f7 http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/7486 http://rdf.disgenet.org/resource/gda/DGNf925e88b432af4c2c3fb5ab7c1a015f7 http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C4275075 http://rdf.disgenet.org/resource/gda/DGNf925e88b432af4c2c3fb5ab7c1a015f7 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP1116827.RAxxFxTFylKfNYCbYpIBFiHmB_FtGBE-cjxk8TufN2HnM#provenance http://rdf.disgenet.org/resource/nanopub/NP1116827.RAxxFxTFylKfNYCbYpIBFiHmB_FtGBE-cjxk8TufN2HnM#assertion http://purl.org/dc/terms/description [We report on a familial case of atypical Werner syndrome (a progeroid syndrome with Werner syndrome phenotype but without typical RECQL2 mutation) presenting with acute ischemic cerebral disease or peripheral artery disease associated with diffuse atherosclerosis, attributable to transmission of a novel LMNA mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP1116827.RAxxFxTFylKfNYCbYpIBFiHmB_FtGBE-cjxk8TufN2HnM#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/NP1116827.RAxxFxTFylKfNYCbYpIBFiHmB_FtGBE-cjxk8TufN2HnM#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/19095983 http://rdf.disgenet.org/resource/nanopub/NP1116827.RAxxFxTFylKfNYCbYpIBFiHmB_FtGBE-cjxk8TufN2HnM#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP1116827.RAxxFxTFylKfNYCbYpIBFiHmB_FtGBE-cjxk8TufN2HnM#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/NP1116827.RAxxFxTFylKfNYCbYpIBFiHmB_FtGBE-cjxk8TufN2HnM#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP1116827.RAxxFxTFylKfNYCbYpIBFiHmB_FtGBE-cjxk8TufN2HnM http://purl.org/dc/terms/created 2017-10-17T13:17:18+02:00 http://rdf.disgenet.org/resource/nanopub/NP1116827.RAxxFxTFylKfNYCbYpIBFiHmB_FtGBE-cjxk8TufN2HnM http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP1116827.RAxxFxTFylKfNYCbYpIBFiHmB_FtGBE-cjxk8TufN2HnM http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP1116827.RAxxFxTFylKfNYCbYpIBFiHmB_FtGBE-cjxk8TufN2HnM http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP1116827.RAxxFxTFylKfNYCbYpIBFiHmB_FtGBE-cjxk8TufN2HnM http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP1116827.RAxxFxTFylKfNYCbYpIBFiHmB_FtGBE-cjxk8TufN2HnM http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP1116827.RAxxFxTFylKfNYCbYpIBFiHmB_FtGBE-cjxk8TufN2HnM http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP1116827.RAxxFxTFylKfNYCbYpIBFiHmB_FtGBE-cjxk8TufN2HnM http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP1116827.RAxxFxTFylKfNYCbYpIBFiHmB_FtGBE-cjxk8TufN2HnM http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP1116827.RAxxFxTFylKfNYCbYpIBFiHmB_FtGBE-cjxk8TufN2HnM http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP1116827.RAxxFxTFylKfNYCbYpIBFiHmB_FtGBE-cjxk8TufN2HnM http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP1116827.RAxxFxTFylKfNYCbYpIBFiHmB_FtGBE-cjxk8TufN2HnM 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