http://rdf.disgenet.org/resource/nanopub/NP388885.RA9OzzeDoJhXF7nxpRXSPHpTtMskJfJFFox6777ciUBMQ#head http://rdf.disgenet.org/resource/nanopub/NP388885.RA9OzzeDoJhXF7nxpRXSPHpTtMskJfJFFox6777ciUBMQ http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP388885.RA9OzzeDoJhXF7nxpRXSPHpTtMskJfJFFox6777ciUBMQ#assertion http://rdf.disgenet.org/resource/nanopub/NP388885.RA9OzzeDoJhXF7nxpRXSPHpTtMskJfJFFox6777ciUBMQ http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP388885.RA9OzzeDoJhXF7nxpRXSPHpTtMskJfJFFox6777ciUBMQ#provenance http://rdf.disgenet.org/resource/nanopub/NP388885.RA9OzzeDoJhXF7nxpRXSPHpTtMskJfJFFox6777ciUBMQ http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP388885.RA9OzzeDoJhXF7nxpRXSPHpTtMskJfJFFox6777ciUBMQ#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP388885.RA9OzzeDoJhXF7nxpRXSPHpTtMskJfJFFox6777ciUBMQ http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP388885.RA9OzzeDoJhXF7nxpRXSPHpTtMskJfJFFox6777ciUBMQ#assertion http://rdf.disgenet.org/resource/gda/DGN460be1721a187161fb691af8cf3ff613 http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/2200 http://rdf.disgenet.org/resource/gda/DGN460be1721a187161fb691af8cf3ff613 http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0013581 http://rdf.disgenet.org/resource/gda/DGN460be1721a187161fb691af8cf3ff613 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP388885.RA9OzzeDoJhXF7nxpRXSPHpTtMskJfJFFox6777ciUBMQ#provenance http://rdf.disgenet.org/resource/nanopub/NP388885.RA9OzzeDoJhXF7nxpRXSPHpTtMskJfJFFox6777ciUBMQ#assertion http://purl.org/dc/terms/description [Genotype-phenotype analysis revealed that patients with an identified FBN1 mutation were more likely to have ectopia lentis and cardiovascular complications compared to those without an identifiable mutation (relative risks of 4.6 and 1.9, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP388885.RA9OzzeDoJhXF7nxpRXSPHpTtMskJfJFFox6777ciUBMQ#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/NP388885.RA9OzzeDoJhXF7nxpRXSPHpTtMskJfJFFox6777ciUBMQ#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/14695540 http://rdf.disgenet.org/resource/nanopub/NP388885.RA9OzzeDoJhXF7nxpRXSPHpTtMskJfJFFox6777ciUBMQ#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP388885.RA9OzzeDoJhXF7nxpRXSPHpTtMskJfJFFox6777ciUBMQ#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/NP388885.RA9OzzeDoJhXF7nxpRXSPHpTtMskJfJFFox6777ciUBMQ#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP388885.RA9OzzeDoJhXF7nxpRXSPHpTtMskJfJFFox6777ciUBMQ http://purl.org/dc/terms/created 2017-10-17T13:12:39+02:00 http://rdf.disgenet.org/resource/nanopub/NP388885.RA9OzzeDoJhXF7nxpRXSPHpTtMskJfJFFox6777ciUBMQ http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP388885.RA9OzzeDoJhXF7nxpRXSPHpTtMskJfJFFox6777ciUBMQ http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP388885.RA9OzzeDoJhXF7nxpRXSPHpTtMskJfJFFox6777ciUBMQ http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP388885.RA9OzzeDoJhXF7nxpRXSPHpTtMskJfJFFox6777ciUBMQ http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP388885.RA9OzzeDoJhXF7nxpRXSPHpTtMskJfJFFox6777ciUBMQ http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP388885.RA9OzzeDoJhXF7nxpRXSPHpTtMskJfJFFox6777ciUBMQ http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP388885.RA9OzzeDoJhXF7nxpRXSPHpTtMskJfJFFox6777ciUBMQ http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP388885.RA9OzzeDoJhXF7nxpRXSPHpTtMskJfJFFox6777ciUBMQ http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP388885.RA9OzzeDoJhXF7nxpRXSPHpTtMskJfJFFox6777ciUBMQ http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP388885.RA9OzzeDoJhXF7nxpRXSPHpTtMskJfJFFox6777ciUBMQ http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP388885.RA9OzzeDoJhXF7nxpRXSPHpTtMskJfJFFox6777ciUBMQ 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