http://rdf.disgenet.org/resource/nanopub/NP1415160.RAmzhT-RSsu55iNqACpObRjkK7W2BpZyxoNIF_mSgzgX0#head http://rdf.disgenet.org/resource/nanopub/NP1415160.RAmzhT-RSsu55iNqACpObRjkK7W2BpZyxoNIF_mSgzgX0 http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP1415160.RAmzhT-RSsu55iNqACpObRjkK7W2BpZyxoNIF_mSgzgX0#assertion http://rdf.disgenet.org/resource/nanopub/NP1415160.RAmzhT-RSsu55iNqACpObRjkK7W2BpZyxoNIF_mSgzgX0 http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP1415160.RAmzhT-RSsu55iNqACpObRjkK7W2BpZyxoNIF_mSgzgX0#provenance http://rdf.disgenet.org/resource/nanopub/NP1415160.RAmzhT-RSsu55iNqACpObRjkK7W2BpZyxoNIF_mSgzgX0 http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP1415160.RAmzhT-RSsu55iNqACpObRjkK7W2BpZyxoNIF_mSgzgX0#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP1415160.RAmzhT-RSsu55iNqACpObRjkK7W2BpZyxoNIF_mSgzgX0 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP1415160.RAmzhT-RSsu55iNqACpObRjkK7W2BpZyxoNIF_mSgzgX0#assertion http://rdf.disgenet.org/resource/gda/DGN71c353846efe59c31918ab9b0ec28eb2 http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/196527 http://rdf.disgenet.org/resource/gda/DGN71c353846efe59c31918ab9b0ec28eb2 http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0796149 http://rdf.disgenet.org/resource/gda/DGN71c353846efe59c31918ab9b0ec28eb2 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP1415160.RAmzhT-RSsu55iNqACpObRjkK7W2BpZyxoNIF_mSgzgX0#provenance http://rdf.disgenet.org/resource/nanopub/NP1415160.RAmzhT-RSsu55iNqACpObRjkK7W2BpZyxoNIF_mSgzgX0#assertion http://purl.org/dc/terms/description [The excitement about Tmem16 proteins has been enhanced by the finding that Ano1 has been linked to cancer, mutations in Ano5 are linked to several forms of muscular dystrophy (LGMDL2 and MMD-3), mutations in Ano10 are linked to autosomal recessive spinocerebellar ataxia, and mutations in Ano6 are linked to Scott syndrome, a rare bleeding disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP1415160.RAmzhT-RSsu55iNqACpObRjkK7W2BpZyxoNIF_mSgzgX0#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/NP1415160.RAmzhT-RSsu55iNqACpObRjkK7W2BpZyxoNIF_mSgzgX0#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/21642943 http://rdf.disgenet.org/resource/nanopub/NP1415160.RAmzhT-RSsu55iNqACpObRjkK7W2BpZyxoNIF_mSgzgX0#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP1415160.RAmzhT-RSsu55iNqACpObRjkK7W2BpZyxoNIF_mSgzgX0#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/NP1415160.RAmzhT-RSsu55iNqACpObRjkK7W2BpZyxoNIF_mSgzgX0#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP1415160.RAmzhT-RSsu55iNqACpObRjkK7W2BpZyxoNIF_mSgzgX0 http://purl.org/dc/terms/created 2017-10-17T13:19:10+02:00 http://rdf.disgenet.org/resource/nanopub/NP1415160.RAmzhT-RSsu55iNqACpObRjkK7W2BpZyxoNIF_mSgzgX0 http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP1415160.RAmzhT-RSsu55iNqACpObRjkK7W2BpZyxoNIF_mSgzgX0 http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP1415160.RAmzhT-RSsu55iNqACpObRjkK7W2BpZyxoNIF_mSgzgX0 http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP1415160.RAmzhT-RSsu55iNqACpObRjkK7W2BpZyxoNIF_mSgzgX0 http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP1415160.RAmzhT-RSsu55iNqACpObRjkK7W2BpZyxoNIF_mSgzgX0 http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP1415160.RAmzhT-RSsu55iNqACpObRjkK7W2BpZyxoNIF_mSgzgX0 http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP1415160.RAmzhT-RSsu55iNqACpObRjkK7W2BpZyxoNIF_mSgzgX0 http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP1415160.RAmzhT-RSsu55iNqACpObRjkK7W2BpZyxoNIF_mSgzgX0 http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP1415160.RAmzhT-RSsu55iNqACpObRjkK7W2BpZyxoNIF_mSgzgX0 http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP1415160.RAmzhT-RSsu55iNqACpObRjkK7W2BpZyxoNIF_mSgzgX0 http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP1415160.RAmzhT-RSsu55iNqACpObRjkK7W2BpZyxoNIF_mSgzgX0 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