http://rdf.disgenet.org/resource/nanopub/NP303642.RAXNevGD3gRA_plDftnNjGIsSTFb6uyIRtaqb-MT_NXAs#head
http://rdf.disgenet.org/resource/nanopub/NP303642.RAXNevGD3gRA_plDftnNjGIsSTFb6uyIRtaqb-MT_NXAs
http://www.nanopub.org/nschema#hasAssertion
http://rdf.disgenet.org/resource/nanopub/NP303642.RAXNevGD3gRA_plDftnNjGIsSTFb6uyIRtaqb-MT_NXAs#assertion
http://rdf.disgenet.org/resource/nanopub/NP303642.RAXNevGD3gRA_plDftnNjGIsSTFb6uyIRtaqb-MT_NXAs
http://www.nanopub.org/nschema#hasProvenance
http://rdf.disgenet.org/resource/nanopub/NP303642.RAXNevGD3gRA_plDftnNjGIsSTFb6uyIRtaqb-MT_NXAs#provenance
http://rdf.disgenet.org/resource/nanopub/NP303642.RAXNevGD3gRA_plDftnNjGIsSTFb6uyIRtaqb-MT_NXAs
http://www.nanopub.org/nschema#hasPublicationInfo
http://rdf.disgenet.org/resource/nanopub/NP303642.RAXNevGD3gRA_plDftnNjGIsSTFb6uyIRtaqb-MT_NXAs#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP303642.RAXNevGD3gRA_plDftnNjGIsSTFb6uyIRtaqb-MT_NXAs
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://www.nanopub.org/nschema#Nanopublication
http://rdf.disgenet.org/resource/nanopub/NP303642.RAXNevGD3gRA_plDftnNjGIsSTFb6uyIRtaqb-MT_NXAs#assertion
http://rdf.disgenet.org/resource/gda/DGN8404e011e76797fc58a18e825e58c8b0
http://semanticscience.org/resource/SIO_000628
http://identifiers.org/ncbigene/1832
http://rdf.disgenet.org/resource/gda/DGN8404e011e76797fc58a18e825e58c8b0
http://semanticscience.org/resource/SIO_000628
http://linkedlifedata.com/resource/umls/id/C3899989
http://rdf.disgenet.org/resource/gda/DGN8404e011e76797fc58a18e825e58c8b0
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://semanticscience.org/resource/SIO_001122
http://rdf.disgenet.org/resource/nanopub/NP303642.RAXNevGD3gRA_plDftnNjGIsSTFb6uyIRtaqb-MT_NXAs#provenance
http://rdf.disgenet.org/resource/nanopub/NP303642.RAXNevGD3gRA_plDftnNjGIsSTFb6uyIRtaqb-MT_NXAs#assertion
http://purl.org/dc/terms/description
[Recently, mutations in desmoplakin have been shown to underlie some cases of the autosomal dominant disorder, striate palmoplantar keratoderma, as well as an autosomal recessive condition characterized by dilated cardiomyopathy, woolly hair, and keratoderma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
http://rdf.disgenet.org/resource/nanopub/NP303642.RAXNevGD3gRA_plDftnNjGIsSTFb6uyIRtaqb-MT_NXAs#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/NP303642.RAXNevGD3gRA_plDftnNjGIsSTFb6uyIRtaqb-MT_NXAs#assertion
http://semanticscience.org/resource/SIO_000772
http://identifiers.org/pubmed/11841538
http://rdf.disgenet.org/resource/nanopub/NP303642.RAXNevGD3gRA_plDftnNjGIsSTFb6uyIRtaqb-MT_NXAs#assertion
http://www.w3.org/ns/prov#wasDerivedFrom
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://rdf.disgenet.org/resource/nanopub/NP303642.RAXNevGD3gRA_plDftnNjGIsSTFb6uyIRtaqb-MT_NXAs#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/NP303642.RAXNevGD3gRA_plDftnNjGIsSTFb6uyIRtaqb-MT_NXAs#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP303642.RAXNevGD3gRA_plDftnNjGIsSTFb6uyIRtaqb-MT_NXAs
http://purl.org/dc/terms/created
2017-10-17T13:12:06+02:00
http://rdf.disgenet.org/resource/nanopub/NP303642.RAXNevGD3gRA_plDftnNjGIsSTFb6uyIRtaqb-MT_NXAs
http://purl.org/dc/terms/rights
http://opendatacommons.org/licenses/odbl/1.0/
http://rdf.disgenet.org/resource/nanopub/NP303642.RAXNevGD3gRA_plDftnNjGIsSTFb6uyIRtaqb-MT_NXAs
http://purl.org/dc/terms/rightsHolder
http://rdf.disgenet.org/v5.0.0/void/IBIGroup
http://rdf.disgenet.org/resource/nanopub/NP303642.RAXNevGD3gRA_plDftnNjGIsSTFb6uyIRtaqb-MT_NXAs
http://purl.org/dc/terms/subject
http://semanticscience.org/resource/SIO_000983
http://rdf.disgenet.org/resource/nanopub/NP303642.RAXNevGD3gRA_plDftnNjGIsSTFb6uyIRtaqb-MT_NXAs
http://purl.org/net/provenance/ns#usedData
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://rdf.disgenet.org/resource/nanopub/NP303642.RAXNevGD3gRA_plDftnNjGIsSTFb6uyIRtaqb-MT_NXAs
http://purl.org/pav/authoredBy
http://orcid.org/0000-0001-5999-6269
http://rdf.disgenet.org/resource/nanopub/NP303642.RAXNevGD3gRA_plDftnNjGIsSTFb6uyIRtaqb-MT_NXAs
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-7534-7661
http://rdf.disgenet.org/resource/nanopub/NP303642.RAXNevGD3gRA_plDftnNjGIsSTFb6uyIRtaqb-MT_NXAs
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-9383-528X
http://rdf.disgenet.org/resource/nanopub/NP303642.RAXNevGD3gRA_plDftnNjGIsSTFb6uyIRtaqb-MT_NXAs
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP303642.RAXNevGD3gRA_plDftnNjGIsSTFb6uyIRtaqb-MT_NXAs
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-1244-7654
http://rdf.disgenet.org/resource/nanopub/NP303642.RAXNevGD3gRA_plDftnNjGIsSTFb6uyIRtaqb-MT_NXAs
http://purl.org/pav/createdBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP303642.RAXNevGD3gRA_plDftnNjGIsSTFb6uyIRtaqb-MT_NXAs
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