http://rdf.disgenet.org/resource/nanopub/NP290652.RAe92U0Zcx65Aa-ILGi7OsAwlxS2K1eMjnviX8zRzekeY#head http://rdf.disgenet.org/resource/nanopub/NP290652.RAe92U0Zcx65Aa-ILGi7OsAwlxS2K1eMjnviX8zRzekeY http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP290652.RAe92U0Zcx65Aa-ILGi7OsAwlxS2K1eMjnviX8zRzekeY#assertion http://rdf.disgenet.org/resource/nanopub/NP290652.RAe92U0Zcx65Aa-ILGi7OsAwlxS2K1eMjnviX8zRzekeY http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP290652.RAe92U0Zcx65Aa-ILGi7OsAwlxS2K1eMjnviX8zRzekeY#provenance http://rdf.disgenet.org/resource/nanopub/NP290652.RAe92U0Zcx65Aa-ILGi7OsAwlxS2K1eMjnviX8zRzekeY http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP290652.RAe92U0Zcx65Aa-ILGi7OsAwlxS2K1eMjnviX8zRzekeY#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP290652.RAe92U0Zcx65Aa-ILGi7OsAwlxS2K1eMjnviX8zRzekeY http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP290652.RAe92U0Zcx65Aa-ILGi7OsAwlxS2K1eMjnviX8zRzekeY#assertion http://rdf.disgenet.org/resource/gda/DGN30cfd4b8d3898a79f8799a0669c80524 http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/1756 http://rdf.disgenet.org/resource/gda/DGN30cfd4b8d3898a79f8799a0669c80524 http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C1533847 http://rdf.disgenet.org/resource/gda/DGN30cfd4b8d3898a79f8799a0669c80524 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP290652.RAe92U0Zcx65Aa-ILGi7OsAwlxS2K1eMjnviX8zRzekeY#provenance http://rdf.disgenet.org/resource/nanopub/NP290652.RAe92U0Zcx65Aa-ILGi7OsAwlxS2K1eMjnviX8zRzekeY#assertion http://purl.org/dc/terms/description [The first comprehensive mutation scanning of the exons and splice junctions of the dystrophin gene in patients with sporadic DCM presents the evidence that point mutations are associated with sporadic DCM without clinical evidence of skeletal myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP290652.RAe92U0Zcx65Aa-ILGi7OsAwlxS2K1eMjnviX8zRzekeY#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/NP290652.RAe92U0Zcx65Aa-ILGi7OsAwlxS2K1eMjnviX8zRzekeY#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/12359139 http://rdf.disgenet.org/resource/nanopub/NP290652.RAe92U0Zcx65Aa-ILGi7OsAwlxS2K1eMjnviX8zRzekeY#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP290652.RAe92U0Zcx65Aa-ILGi7OsAwlxS2K1eMjnviX8zRzekeY#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/NP290652.RAe92U0Zcx65Aa-ILGi7OsAwlxS2K1eMjnviX8zRzekeY#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP290652.RAe92U0Zcx65Aa-ILGi7OsAwlxS2K1eMjnviX8zRzekeY http://purl.org/dc/terms/created 2017-10-17T13:12:02+02:00 http://rdf.disgenet.org/resource/nanopub/NP290652.RAe92U0Zcx65Aa-ILGi7OsAwlxS2K1eMjnviX8zRzekeY http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP290652.RAe92U0Zcx65Aa-ILGi7OsAwlxS2K1eMjnviX8zRzekeY http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP290652.RAe92U0Zcx65Aa-ILGi7OsAwlxS2K1eMjnviX8zRzekeY http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP290652.RAe92U0Zcx65Aa-ILGi7OsAwlxS2K1eMjnviX8zRzekeY http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP290652.RAe92U0Zcx65Aa-ILGi7OsAwlxS2K1eMjnviX8zRzekeY http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP290652.RAe92U0Zcx65Aa-ILGi7OsAwlxS2K1eMjnviX8zRzekeY http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP290652.RAe92U0Zcx65Aa-ILGi7OsAwlxS2K1eMjnviX8zRzekeY http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP290652.RAe92U0Zcx65Aa-ILGi7OsAwlxS2K1eMjnviX8zRzekeY http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP290652.RAe92U0Zcx65Aa-ILGi7OsAwlxS2K1eMjnviX8zRzekeY http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP290652.RAe92U0Zcx65Aa-ILGi7OsAwlxS2K1eMjnviX8zRzekeY http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP290652.RAe92U0Zcx65Aa-ILGi7OsAwlxS2K1eMjnviX8zRzekeY 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