http://rdf.disgenet.org/resource/nanopub/NP12374.RAuPBHULv6gbs1PQpOXl-as-eIyF9bcoQKfWGFX1_WeOI#head http://rdf.disgenet.org/resource/nanopub/NP12374.RAuPBHULv6gbs1PQpOXl-as-eIyF9bcoQKfWGFX1_WeOI http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP12374.RAuPBHULv6gbs1PQpOXl-as-eIyF9bcoQKfWGFX1_WeOI#assertion http://rdf.disgenet.org/resource/nanopub/NP12374.RAuPBHULv6gbs1PQpOXl-as-eIyF9bcoQKfWGFX1_WeOI http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP12374.RAuPBHULv6gbs1PQpOXl-as-eIyF9bcoQKfWGFX1_WeOI#provenance http://rdf.disgenet.org/resource/nanopub/NP12374.RAuPBHULv6gbs1PQpOXl-as-eIyF9bcoQKfWGFX1_WeOI http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP12374.RAuPBHULv6gbs1PQpOXl-as-eIyF9bcoQKfWGFX1_WeOI#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP12374.RAuPBHULv6gbs1PQpOXl-as-eIyF9bcoQKfWGFX1_WeOI http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP12374.RAuPBHULv6gbs1PQpOXl-as-eIyF9bcoQKfWGFX1_WeOI#assertion http://rdf.disgenet.org/resource/gda/DGN5fdaf48a099143f93dfbf015b131efa1 http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/100 http://rdf.disgenet.org/resource/gda/DGN5fdaf48a099143f93dfbf015b131efa1 http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0037277 http://rdf.disgenet.org/resource/gda/DGN5fdaf48a099143f93dfbf015b131efa1 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP12374.RAuPBHULv6gbs1PQpOXl-as-eIyF9bcoQKfWGFX1_WeOI#provenance http://rdf.disgenet.org/resource/nanopub/NP12374.RAuPBHULv6gbs1PQpOXl-as-eIyF9bcoQKfWGFX1_WeOI#assertion http://purl.org/dc/terms/description [Dyschromatosis symmetrica hereditaria (DSH) is an autosomal dominant pigmentary genodermatosis characterized by hyperpigmented and hypopigmented macules of on the extremities and caused by the mutations in the ADAR gene(also called DSRAD) encoding for RNA-specific adenosine deaminase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP12374.RAuPBHULv6gbs1PQpOXl-as-eIyF9bcoQKfWGFX1_WeOI#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/NP12374.RAuPBHULv6gbs1PQpOXl-as-eIyF9bcoQKfWGFX1_WeOI#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/15146470 http://rdf.disgenet.org/resource/nanopub/NP12374.RAuPBHULv6gbs1PQpOXl-as-eIyF9bcoQKfWGFX1_WeOI#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP12374.RAuPBHULv6gbs1PQpOXl-as-eIyF9bcoQKfWGFX1_WeOI#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/NP12374.RAuPBHULv6gbs1PQpOXl-as-eIyF9bcoQKfWGFX1_WeOI#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP12374.RAuPBHULv6gbs1PQpOXl-as-eIyF9bcoQKfWGFX1_WeOI http://purl.org/dc/terms/created 2017-10-17T13:10:16+02:00 http://rdf.disgenet.org/resource/nanopub/NP12374.RAuPBHULv6gbs1PQpOXl-as-eIyF9bcoQKfWGFX1_WeOI http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP12374.RAuPBHULv6gbs1PQpOXl-as-eIyF9bcoQKfWGFX1_WeOI http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP12374.RAuPBHULv6gbs1PQpOXl-as-eIyF9bcoQKfWGFX1_WeOI http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP12374.RAuPBHULv6gbs1PQpOXl-as-eIyF9bcoQKfWGFX1_WeOI http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP12374.RAuPBHULv6gbs1PQpOXl-as-eIyF9bcoQKfWGFX1_WeOI http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP12374.RAuPBHULv6gbs1PQpOXl-as-eIyF9bcoQKfWGFX1_WeOI http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP12374.RAuPBHULv6gbs1PQpOXl-as-eIyF9bcoQKfWGFX1_WeOI http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP12374.RAuPBHULv6gbs1PQpOXl-as-eIyF9bcoQKfWGFX1_WeOI http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP12374.RAuPBHULv6gbs1PQpOXl-as-eIyF9bcoQKfWGFX1_WeOI http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP12374.RAuPBHULv6gbs1PQpOXl-as-eIyF9bcoQKfWGFX1_WeOI http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP12374.RAuPBHULv6gbs1PQpOXl-as-eIyF9bcoQKfWGFX1_WeOI 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