http://rdf.disgenet.org/resource/nanopub/NP291745.RAiQPqmA1HNVK10ov5lm0prOVl1JAa43gH4Q5tP-RVybw#head http://rdf.disgenet.org/resource/nanopub/NP291745.RAiQPqmA1HNVK10ov5lm0prOVl1JAa43gH4Q5tP-RVybw http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP291745.RAiQPqmA1HNVK10ov5lm0prOVl1JAa43gH4Q5tP-RVybw#assertion http://rdf.disgenet.org/resource/nanopub/NP291745.RAiQPqmA1HNVK10ov5lm0prOVl1JAa43gH4Q5tP-RVybw http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP291745.RAiQPqmA1HNVK10ov5lm0prOVl1JAa43gH4Q5tP-RVybw#provenance http://rdf.disgenet.org/resource/nanopub/NP291745.RAiQPqmA1HNVK10ov5lm0prOVl1JAa43gH4Q5tP-RVybw http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP291745.RAiQPqmA1HNVK10ov5lm0prOVl1JAa43gH4Q5tP-RVybw#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP291745.RAiQPqmA1HNVK10ov5lm0prOVl1JAa43gH4Q5tP-RVybw http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP291745.RAiQPqmA1HNVK10ov5lm0prOVl1JAa43gH4Q5tP-RVybw#assertion http://rdf.disgenet.org/resource/gda/DGNfcee005f6ac6395f73d89f211576648b http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/1756 http://rdf.disgenet.org/resource/gda/DGNfcee005f6ac6395f73d89f211576648b http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0013264 http://rdf.disgenet.org/resource/gda/DGNfcee005f6ac6395f73d89f211576648b http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP291745.RAiQPqmA1HNVK10ov5lm0prOVl1JAa43gH4Q5tP-RVybw#provenance http://rdf.disgenet.org/resource/nanopub/NP291745.RAiQPqmA1HNVK10ov5lm0prOVl1JAa43gH4Q5tP-RVybw#assertion http://purl.org/dc/terms/description [Duchenne muscular dystrophy (DMD) is associated with mutations in the dystrophin gene that disrupt the open reading frame whereas the milder Becker's form is associated with mutations which leave an in-frame mRNA transcript that can be translated into a protein that includes the N- and C- terminal functional domains.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP291745.RAiQPqmA1HNVK10ov5lm0prOVl1JAa43gH4Q5tP-RVybw#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/NP291745.RAiQPqmA1HNVK10ov5lm0prOVl1JAa43gH4Q5tP-RVybw#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/20978473 http://rdf.disgenet.org/resource/nanopub/NP291745.RAiQPqmA1HNVK10ov5lm0prOVl1JAa43gH4Q5tP-RVybw#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP291745.RAiQPqmA1HNVK10ov5lm0prOVl1JAa43gH4Q5tP-RVybw#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/NP291745.RAiQPqmA1HNVK10ov5lm0prOVl1JAa43gH4Q5tP-RVybw#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP291745.RAiQPqmA1HNVK10ov5lm0prOVl1JAa43gH4Q5tP-RVybw http://purl.org/dc/terms/created 2017-10-17T13:12:02+02:00 http://rdf.disgenet.org/resource/nanopub/NP291745.RAiQPqmA1HNVK10ov5lm0prOVl1JAa43gH4Q5tP-RVybw http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP291745.RAiQPqmA1HNVK10ov5lm0prOVl1JAa43gH4Q5tP-RVybw http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP291745.RAiQPqmA1HNVK10ov5lm0prOVl1JAa43gH4Q5tP-RVybw http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP291745.RAiQPqmA1HNVK10ov5lm0prOVl1JAa43gH4Q5tP-RVybw http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP291745.RAiQPqmA1HNVK10ov5lm0prOVl1JAa43gH4Q5tP-RVybw http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP291745.RAiQPqmA1HNVK10ov5lm0prOVl1JAa43gH4Q5tP-RVybw http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP291745.RAiQPqmA1HNVK10ov5lm0prOVl1JAa43gH4Q5tP-RVybw http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP291745.RAiQPqmA1HNVK10ov5lm0prOVl1JAa43gH4Q5tP-RVybw http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP291745.RAiQPqmA1HNVK10ov5lm0prOVl1JAa43gH4Q5tP-RVybw http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP291745.RAiQPqmA1HNVK10ov5lm0prOVl1JAa43gH4Q5tP-RVybw http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP291745.RAiQPqmA1HNVK10ov5lm0prOVl1JAa43gH4Q5tP-RVybw 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