http://rdf.disgenet.org/resource/nanopub/NP1169622.RAquSKtvWucccnU6s9N1y90vhC2Ig0kVTAnYTa46KGQ38#head http://rdf.disgenet.org/resource/nanopub/NP1169622.RAquSKtvWucccnU6s9N1y90vhC2Ig0kVTAnYTa46KGQ38 http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP1169622.RAquSKtvWucccnU6s9N1y90vhC2Ig0kVTAnYTa46KGQ38#assertion http://rdf.disgenet.org/resource/nanopub/NP1169622.RAquSKtvWucccnU6s9N1y90vhC2Ig0kVTAnYTa46KGQ38 http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP1169622.RAquSKtvWucccnU6s9N1y90vhC2Ig0kVTAnYTa46KGQ38#provenance http://rdf.disgenet.org/resource/nanopub/NP1169622.RAquSKtvWucccnU6s9N1y90vhC2Ig0kVTAnYTa46KGQ38 http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP1169622.RAquSKtvWucccnU6s9N1y90vhC2Ig0kVTAnYTa46KGQ38#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP1169622.RAquSKtvWucccnU6s9N1y90vhC2Ig0kVTAnYTa46KGQ38 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP1169622.RAquSKtvWucccnU6s9N1y90vhC2Ig0kVTAnYTa46KGQ38#assertion http://rdf.disgenet.org/resource/gda/DGNecefea07633c6b59e437c29403618144 http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/8988 http://rdf.disgenet.org/resource/gda/DGNecefea07633c6b59e437c29403618144 http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0007959 http://rdf.disgenet.org/resource/gda/DGNecefea07633c6b59e437c29403618144 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP1169622.RAquSKtvWucccnU6s9N1y90vhC2Ig0kVTAnYTa46KGQ38#provenance http://rdf.disgenet.org/resource/nanopub/NP1169622.RAquSKtvWucccnU6s9N1y90vhC2Ig0kVTAnYTa46KGQ38#assertion http://purl.org/dc/terms/description [Recently, mutations in both the small heat shock protein 27 (HSP27 or HSPB1) and 22 (HSP22 or HSPB8) genes have been reported to cause autosomal dominant CMT with minimal sensory involvement (CMT 2F/CMT2L) and autosomal dominant distal hereditary motor neuropathy type II (dHMN II).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP1169622.RAquSKtvWucccnU6s9N1y90vhC2Ig0kVTAnYTa46KGQ38#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/NP1169622.RAquSKtvWucccnU6s9N1y90vhC2Ig0kVTAnYTa46KGQ38#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/18832141 http://rdf.disgenet.org/resource/nanopub/NP1169622.RAquSKtvWucccnU6s9N1y90vhC2Ig0kVTAnYTa46KGQ38#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP1169622.RAquSKtvWucccnU6s9N1y90vhC2Ig0kVTAnYTa46KGQ38#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/NP1169622.RAquSKtvWucccnU6s9N1y90vhC2Ig0kVTAnYTa46KGQ38#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP1169622.RAquSKtvWucccnU6s9N1y90vhC2Ig0kVTAnYTa46KGQ38 http://purl.org/dc/terms/created 2017-10-17T13:17:38+02:00 http://rdf.disgenet.org/resource/nanopub/NP1169622.RAquSKtvWucccnU6s9N1y90vhC2Ig0kVTAnYTa46KGQ38 http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP1169622.RAquSKtvWucccnU6s9N1y90vhC2Ig0kVTAnYTa46KGQ38 http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP1169622.RAquSKtvWucccnU6s9N1y90vhC2Ig0kVTAnYTa46KGQ38 http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP1169622.RAquSKtvWucccnU6s9N1y90vhC2Ig0kVTAnYTa46KGQ38 http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP1169622.RAquSKtvWucccnU6s9N1y90vhC2Ig0kVTAnYTa46KGQ38 http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP1169622.RAquSKtvWucccnU6s9N1y90vhC2Ig0kVTAnYTa46KGQ38 http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP1169622.RAquSKtvWucccnU6s9N1y90vhC2Ig0kVTAnYTa46KGQ38 http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP1169622.RAquSKtvWucccnU6s9N1y90vhC2Ig0kVTAnYTa46KGQ38 http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP1169622.RAquSKtvWucccnU6s9N1y90vhC2Ig0kVTAnYTa46KGQ38 http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP1169622.RAquSKtvWucccnU6s9N1y90vhC2Ig0kVTAnYTa46KGQ38 http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP1169622.RAquSKtvWucccnU6s9N1y90vhC2Ig0kVTAnYTa46KGQ38 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