http://rdf.disgenet.org/resource/nanopub/NP292721.RA60lPEM2ATNyGqE0za5opw2-ghrJ2df2M-mEzgIyFJNc#head
http://rdf.disgenet.org/resource/nanopub/NP292721.RA60lPEM2ATNyGqE0za5opw2-ghrJ2df2M-mEzgIyFJNc
http://www.nanopub.org/nschema#hasAssertion
http://rdf.disgenet.org/resource/nanopub/NP292721.RA60lPEM2ATNyGqE0za5opw2-ghrJ2df2M-mEzgIyFJNc#assertion
http://rdf.disgenet.org/resource/nanopub/NP292721.RA60lPEM2ATNyGqE0za5opw2-ghrJ2df2M-mEzgIyFJNc
http://www.nanopub.org/nschema#hasProvenance
http://rdf.disgenet.org/resource/nanopub/NP292721.RA60lPEM2ATNyGqE0za5opw2-ghrJ2df2M-mEzgIyFJNc#provenance
http://rdf.disgenet.org/resource/nanopub/NP292721.RA60lPEM2ATNyGqE0za5opw2-ghrJ2df2M-mEzgIyFJNc
http://www.nanopub.org/nschema#hasPublicationInfo
http://rdf.disgenet.org/resource/nanopub/NP292721.RA60lPEM2ATNyGqE0za5opw2-ghrJ2df2M-mEzgIyFJNc#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP292721.RA60lPEM2ATNyGqE0za5opw2-ghrJ2df2M-mEzgIyFJNc
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://www.nanopub.org/nschema#Nanopublication
http://rdf.disgenet.org/resource/nanopub/NP292721.RA60lPEM2ATNyGqE0za5opw2-ghrJ2df2M-mEzgIyFJNc#assertion
http://rdf.disgenet.org/resource/gda/DGNcb55a162e103c69bfa5cf04b743b1a54
http://semanticscience.org/resource/SIO_000628
http://identifiers.org/ncbigene/1756
http://rdf.disgenet.org/resource/gda/DGNcb55a162e103c69bfa5cf04b743b1a54
http://semanticscience.org/resource/SIO_000628
http://linkedlifedata.com/resource/umls/id/C0917713
http://rdf.disgenet.org/resource/gda/DGNcb55a162e103c69bfa5cf04b743b1a54
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://semanticscience.org/resource/SIO_001122
http://rdf.disgenet.org/resource/nanopub/NP292721.RA60lPEM2ATNyGqE0za5opw2-ghrJ2df2M-mEzgIyFJNc#provenance
http://rdf.disgenet.org/resource/nanopub/NP292721.RA60lPEM2ATNyGqE0za5opw2-ghrJ2df2M-mEzgIyFJNc#assertion
http://purl.org/dc/terms/description
[Neither female Duchenne muscular dystrophy (DMD) nor BMD due to homozygous dystrophin mutation has ever been identified although female DMD has been found in patients with Turner syndrome or unilateral parental disomy for X chromosome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
http://rdf.disgenet.org/resource/nanopub/NP292721.RA60lPEM2ATNyGqE0za5opw2-ghrJ2df2M-mEzgIyFJNc#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/NP292721.RA60lPEM2ATNyGqE0za5opw2-ghrJ2df2M-mEzgIyFJNc#assertion
http://semanticscience.org/resource/SIO_000772
http://identifiers.org/pubmed/19396825
http://rdf.disgenet.org/resource/nanopub/NP292721.RA60lPEM2ATNyGqE0za5opw2-ghrJ2df2M-mEzgIyFJNc#assertion
http://www.w3.org/ns/prov#wasDerivedFrom
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://rdf.disgenet.org/resource/nanopub/NP292721.RA60lPEM2ATNyGqE0za5opw2-ghrJ2df2M-mEzgIyFJNc#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/NP292721.RA60lPEM2ATNyGqE0za5opw2-ghrJ2df2M-mEzgIyFJNc#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP292721.RA60lPEM2ATNyGqE0za5opw2-ghrJ2df2M-mEzgIyFJNc
http://purl.org/dc/terms/created
2017-10-17T13:12:03+02:00
http://rdf.disgenet.org/resource/nanopub/NP292721.RA60lPEM2ATNyGqE0za5opw2-ghrJ2df2M-mEzgIyFJNc
http://purl.org/dc/terms/rights
http://opendatacommons.org/licenses/odbl/1.0/
http://rdf.disgenet.org/resource/nanopub/NP292721.RA60lPEM2ATNyGqE0za5opw2-ghrJ2df2M-mEzgIyFJNc
http://purl.org/dc/terms/rightsHolder
http://rdf.disgenet.org/v5.0.0/void/IBIGroup
http://rdf.disgenet.org/resource/nanopub/NP292721.RA60lPEM2ATNyGqE0za5opw2-ghrJ2df2M-mEzgIyFJNc
http://purl.org/dc/terms/subject
http://semanticscience.org/resource/SIO_000983
http://rdf.disgenet.org/resource/nanopub/NP292721.RA60lPEM2ATNyGqE0za5opw2-ghrJ2df2M-mEzgIyFJNc
http://purl.org/net/provenance/ns#usedData
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://rdf.disgenet.org/resource/nanopub/NP292721.RA60lPEM2ATNyGqE0za5opw2-ghrJ2df2M-mEzgIyFJNc
http://purl.org/pav/authoredBy
http://orcid.org/0000-0001-5999-6269
http://rdf.disgenet.org/resource/nanopub/NP292721.RA60lPEM2ATNyGqE0za5opw2-ghrJ2df2M-mEzgIyFJNc
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-7534-7661
http://rdf.disgenet.org/resource/nanopub/NP292721.RA60lPEM2ATNyGqE0za5opw2-ghrJ2df2M-mEzgIyFJNc
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-9383-528X
http://rdf.disgenet.org/resource/nanopub/NP292721.RA60lPEM2ATNyGqE0za5opw2-ghrJ2df2M-mEzgIyFJNc
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP292721.RA60lPEM2ATNyGqE0za5opw2-ghrJ2df2M-mEzgIyFJNc
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-1244-7654
http://rdf.disgenet.org/resource/nanopub/NP292721.RA60lPEM2ATNyGqE0za5opw2-ghrJ2df2M-mEzgIyFJNc
http://purl.org/pav/createdBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP292721.RA60lPEM2ATNyGqE0za5opw2-ghrJ2df2M-mEzgIyFJNc
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