http://rdf.disgenet.org/resource/nanopub/NP291360.RA9o5gmKjKvylKMwqBEwj1yvKrzS8FPLvzHBqSOJnYb9s#head http://rdf.disgenet.org/resource/nanopub/NP291360.RA9o5gmKjKvylKMwqBEwj1yvKrzS8FPLvzHBqSOJnYb9s http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP291360.RA9o5gmKjKvylKMwqBEwj1yvKrzS8FPLvzHBqSOJnYb9s#assertion http://rdf.disgenet.org/resource/nanopub/NP291360.RA9o5gmKjKvylKMwqBEwj1yvKrzS8FPLvzHBqSOJnYb9s http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP291360.RA9o5gmKjKvylKMwqBEwj1yvKrzS8FPLvzHBqSOJnYb9s#provenance http://rdf.disgenet.org/resource/nanopub/NP291360.RA9o5gmKjKvylKMwqBEwj1yvKrzS8FPLvzHBqSOJnYb9s http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP291360.RA9o5gmKjKvylKMwqBEwj1yvKrzS8FPLvzHBqSOJnYb9s#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP291360.RA9o5gmKjKvylKMwqBEwj1yvKrzS8FPLvzHBqSOJnYb9s http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP291360.RA9o5gmKjKvylKMwqBEwj1yvKrzS8FPLvzHBqSOJnYb9s#assertion http://rdf.disgenet.org/resource/gda/DGN40506e8bf57138b7d46e56be7ae8a582 http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/1756 http://rdf.disgenet.org/resource/gda/DGN40506e8bf57138b7d46e56be7ae8a582 http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0043046 http://rdf.disgenet.org/resource/gda/DGN40506e8bf57138b7d46e56be7ae8a582 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP291360.RA9o5gmKjKvylKMwqBEwj1yvKrzS8FPLvzHBqSOJnYb9s#provenance http://rdf.disgenet.org/resource/nanopub/NP291360.RA9o5gmKjKvylKMwqBEwj1yvKrzS8FPLvzHBqSOJnYb9s#assertion http://purl.org/dc/terms/description [Out of three mutations in the dystrophin gene that cause Duchenne muscular dystrophy (DMD), the most common, serious childhood muscle wasting disease, two are genomic deletions of one or more exons that disrupt the reading frame.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP291360.RA9o5gmKjKvylKMwqBEwj1yvKrzS8FPLvzHBqSOJnYb9s#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/NP291360.RA9o5gmKjKvylKMwqBEwj1yvKrzS8FPLvzHBqSOJnYb9s#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/18570328 http://rdf.disgenet.org/resource/nanopub/NP291360.RA9o5gmKjKvylKMwqBEwj1yvKrzS8FPLvzHBqSOJnYb9s#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP291360.RA9o5gmKjKvylKMwqBEwj1yvKrzS8FPLvzHBqSOJnYb9s#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/NP291360.RA9o5gmKjKvylKMwqBEwj1yvKrzS8FPLvzHBqSOJnYb9s#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP291360.RA9o5gmKjKvylKMwqBEwj1yvKrzS8FPLvzHBqSOJnYb9s http://purl.org/dc/terms/created 2017-10-17T13:12:02+02:00 http://rdf.disgenet.org/resource/nanopub/NP291360.RA9o5gmKjKvylKMwqBEwj1yvKrzS8FPLvzHBqSOJnYb9s http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP291360.RA9o5gmKjKvylKMwqBEwj1yvKrzS8FPLvzHBqSOJnYb9s http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP291360.RA9o5gmKjKvylKMwqBEwj1yvKrzS8FPLvzHBqSOJnYb9s http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP291360.RA9o5gmKjKvylKMwqBEwj1yvKrzS8FPLvzHBqSOJnYb9s http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP291360.RA9o5gmKjKvylKMwqBEwj1yvKrzS8FPLvzHBqSOJnYb9s http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP291360.RA9o5gmKjKvylKMwqBEwj1yvKrzS8FPLvzHBqSOJnYb9s http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP291360.RA9o5gmKjKvylKMwqBEwj1yvKrzS8FPLvzHBqSOJnYb9s http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP291360.RA9o5gmKjKvylKMwqBEwj1yvKrzS8FPLvzHBqSOJnYb9s http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP291360.RA9o5gmKjKvylKMwqBEwj1yvKrzS8FPLvzHBqSOJnYb9s http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP291360.RA9o5gmKjKvylKMwqBEwj1yvKrzS8FPLvzHBqSOJnYb9s http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP291360.RA9o5gmKjKvylKMwqBEwj1yvKrzS8FPLvzHBqSOJnYb9s 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