http://rdf.disgenet.org/resource/nanopub/NP834290.RAm7zAfOu8tExlwr7rCHbH6WQ9Zhp5XSWirEvbkNBW4e4#head http://rdf.disgenet.org/resource/nanopub/NP834290.RAm7zAfOu8tExlwr7rCHbH6WQ9Zhp5XSWirEvbkNBW4e4 http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP834290.RAm7zAfOu8tExlwr7rCHbH6WQ9Zhp5XSWirEvbkNBW4e4#assertion http://rdf.disgenet.org/resource/nanopub/NP834290.RAm7zAfOu8tExlwr7rCHbH6WQ9Zhp5XSWirEvbkNBW4e4 http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP834290.RAm7zAfOu8tExlwr7rCHbH6WQ9Zhp5XSWirEvbkNBW4e4#provenance http://rdf.disgenet.org/resource/nanopub/NP834290.RAm7zAfOu8tExlwr7rCHbH6WQ9Zhp5XSWirEvbkNBW4e4 http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP834290.RAm7zAfOu8tExlwr7rCHbH6WQ9Zhp5XSWirEvbkNBW4e4#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP834290.RAm7zAfOu8tExlwr7rCHbH6WQ9Zhp5XSWirEvbkNBW4e4 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP834290.RAm7zAfOu8tExlwr7rCHbH6WQ9Zhp5XSWirEvbkNBW4e4#assertion http://rdf.disgenet.org/resource/gda/DGN00f6000b697af199e46c83fabf0b1be7 http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/5376 http://rdf.disgenet.org/resource/gda/DGN00f6000b697af199e46c83fabf0b1be7 http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C1834304 http://rdf.disgenet.org/resource/gda/DGN00f6000b697af199e46c83fabf0b1be7 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP834290.RAm7zAfOu8tExlwr7rCHbH6WQ9Zhp5XSWirEvbkNBW4e4#provenance http://rdf.disgenet.org/resource/nanopub/NP834290.RAm7zAfOu8tExlwr7rCHbH6WQ9Zhp5XSWirEvbkNBW4e4#assertion http://purl.org/dc/terms/description [Disorders with a known molecular basis falling within this group include hereditary neuropathy with liability to pressure palsies (HNPP) due to the deletion of the PMP22 gene or to mutations in this same gene, and hereditary neuralgic amyotrophy (HNA) caused by mutations in the SEPT9 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP834290.RAm7zAfOu8tExlwr7rCHbH6WQ9Zhp5XSWirEvbkNBW4e4#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/NP834290.RAm7zAfOu8tExlwr7rCHbH6WQ9Zhp5XSWirEvbkNBW4e4#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/24878226 http://rdf.disgenet.org/resource/nanopub/NP834290.RAm7zAfOu8tExlwr7rCHbH6WQ9Zhp5XSWirEvbkNBW4e4#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP834290.RAm7zAfOu8tExlwr7rCHbH6WQ9Zhp5XSWirEvbkNBW4e4#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/NP834290.RAm7zAfOu8tExlwr7rCHbH6WQ9Zhp5XSWirEvbkNBW4e4#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP834290.RAm7zAfOu8tExlwr7rCHbH6WQ9Zhp5XSWirEvbkNBW4e4 http://purl.org/dc/terms/created 2017-10-17T13:15:30+02:00 http://rdf.disgenet.org/resource/nanopub/NP834290.RAm7zAfOu8tExlwr7rCHbH6WQ9Zhp5XSWirEvbkNBW4e4 http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP834290.RAm7zAfOu8tExlwr7rCHbH6WQ9Zhp5XSWirEvbkNBW4e4 http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP834290.RAm7zAfOu8tExlwr7rCHbH6WQ9Zhp5XSWirEvbkNBW4e4 http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP834290.RAm7zAfOu8tExlwr7rCHbH6WQ9Zhp5XSWirEvbkNBW4e4 http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP834290.RAm7zAfOu8tExlwr7rCHbH6WQ9Zhp5XSWirEvbkNBW4e4 http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP834290.RAm7zAfOu8tExlwr7rCHbH6WQ9Zhp5XSWirEvbkNBW4e4 http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP834290.RAm7zAfOu8tExlwr7rCHbH6WQ9Zhp5XSWirEvbkNBW4e4 http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP834290.RAm7zAfOu8tExlwr7rCHbH6WQ9Zhp5XSWirEvbkNBW4e4 http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP834290.RAm7zAfOu8tExlwr7rCHbH6WQ9Zhp5XSWirEvbkNBW4e4 http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP834290.RAm7zAfOu8tExlwr7rCHbH6WQ9Zhp5XSWirEvbkNBW4e4 http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP834290.RAm7zAfOu8tExlwr7rCHbH6WQ9Zhp5XSWirEvbkNBW4e4 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