http://rdf.disgenet.org/resource/nanopub/NP1116760.RAZZINSDd2pJdpZu-u35sa_Q1DEkmosfCyDioWI7X_NIM#head http://rdf.disgenet.org/resource/nanopub/NP1116760.RAZZINSDd2pJdpZu-u35sa_Q1DEkmosfCyDioWI7X_NIM http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP1116760.RAZZINSDd2pJdpZu-u35sa_Q1DEkmosfCyDioWI7X_NIM#assertion http://rdf.disgenet.org/resource/nanopub/NP1116760.RAZZINSDd2pJdpZu-u35sa_Q1DEkmosfCyDioWI7X_NIM http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP1116760.RAZZINSDd2pJdpZu-u35sa_Q1DEkmosfCyDioWI7X_NIM#provenance http://rdf.disgenet.org/resource/nanopub/NP1116760.RAZZINSDd2pJdpZu-u35sa_Q1DEkmosfCyDioWI7X_NIM http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP1116760.RAZZINSDd2pJdpZu-u35sa_Q1DEkmosfCyDioWI7X_NIM#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP1116760.RAZZINSDd2pJdpZu-u35sa_Q1DEkmosfCyDioWI7X_NIM http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP1116760.RAZZINSDd2pJdpZu-u35sa_Q1DEkmosfCyDioWI7X_NIM#assertion http://rdf.disgenet.org/resource/gda/DGN46b210730cde08f715837baf77394a51 http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/7486 http://rdf.disgenet.org/resource/gda/DGN46b210730cde08f715837baf77394a51 http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C1704436 http://rdf.disgenet.org/resource/gda/DGN46b210730cde08f715837baf77394a51 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP1116760.RAZZINSDd2pJdpZu-u35sa_Q1DEkmosfCyDioWI7X_NIM#provenance http://rdf.disgenet.org/resource/nanopub/NP1116760.RAZZINSDd2pJdpZu-u35sa_Q1DEkmosfCyDioWI7X_NIM#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/NP1116760.RAZZINSDd2pJdpZu-u35sa_Q1DEkmosfCyDioWI7X_NIM#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/NP1116760.RAZZINSDd2pJdpZu-u35sa_Q1DEkmosfCyDioWI7X_NIM#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/19095983 http://rdf.disgenet.org/resource/nanopub/NP1116760.RAZZINSDd2pJdpZu-u35sa_Q1DEkmosfCyDioWI7X_NIM#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP1116760.RAZZINSDd2pJdpZu-u35sa_Q1DEkmosfCyDioWI7X_NIM#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/NP1116760.RAZZINSDd2pJdpZu-u35sa_Q1DEkmosfCyDioWI7X_NIM#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP1116760.RAZZINSDd2pJdpZu-u35sa_Q1DEkmosfCyDioWI7X_NIM http://purl.org/dc/terms/created 2017-10-17T13:17:18+02:00 http://rdf.disgenet.org/resource/nanopub/NP1116760.RAZZINSDd2pJdpZu-u35sa_Q1DEkmosfCyDioWI7X_NIM http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP1116760.RAZZINSDd2pJdpZu-u35sa_Q1DEkmosfCyDioWI7X_NIM http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP1116760.RAZZINSDd2pJdpZu-u35sa_Q1DEkmosfCyDioWI7X_NIM http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP1116760.RAZZINSDd2pJdpZu-u35sa_Q1DEkmosfCyDioWI7X_NIM http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP1116760.RAZZINSDd2pJdpZu-u35sa_Q1DEkmosfCyDioWI7X_NIM http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP1116760.RAZZINSDd2pJdpZu-u35sa_Q1DEkmosfCyDioWI7X_NIM http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP1116760.RAZZINSDd2pJdpZu-u35sa_Q1DEkmosfCyDioWI7X_NIM http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP1116760.RAZZINSDd2pJdpZu-u35sa_Q1DEkmosfCyDioWI7X_NIM http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP1116760.RAZZINSDd2pJdpZu-u35sa_Q1DEkmosfCyDioWI7X_NIM http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP1116760.RAZZINSDd2pJdpZu-u35sa_Q1DEkmosfCyDioWI7X_NIM http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP1116760.RAZZINSDd2pJdpZu-u35sa_Q1DEkmosfCyDioWI7X_NIM 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