http://rdf.disgenet.org/resource/nanopub/NP1010927.RAq0_lRZA_My9iS1BNRomKHP_mE0hFe5uFNOGP3D4DT2E#head http://rdf.disgenet.org/resource/nanopub/NP1010927.RAq0_lRZA_My9iS1BNRomKHP_mE0hFe5uFNOGP3D4DT2E http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP1010927.RAq0_lRZA_My9iS1BNRomKHP_mE0hFe5uFNOGP3D4DT2E#assertion http://rdf.disgenet.org/resource/nanopub/NP1010927.RAq0_lRZA_My9iS1BNRomKHP_mE0hFe5uFNOGP3D4DT2E http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP1010927.RAq0_lRZA_My9iS1BNRomKHP_mE0hFe5uFNOGP3D4DT2E#provenance http://rdf.disgenet.org/resource/nanopub/NP1010927.RAq0_lRZA_My9iS1BNRomKHP_mE0hFe5uFNOGP3D4DT2E http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP1010927.RAq0_lRZA_My9iS1BNRomKHP_mE0hFe5uFNOGP3D4DT2E#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP1010927.RAq0_lRZA_My9iS1BNRomKHP_mE0hFe5uFNOGP3D4DT2E http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP1010927.RAq0_lRZA_My9iS1BNRomKHP_mE0hFe5uFNOGP3D4DT2E#assertion http://rdf.disgenet.org/resource/gda/DGN54071fefc94048d83aea5a9180e4a240 http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/7036 http://rdf.disgenet.org/resource/gda/DGN54071fefc94048d83aea5a9180e4a240 http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C1858664 http://rdf.disgenet.org/resource/gda/DGN54071fefc94048d83aea5a9180e4a240 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP1010927.RAq0_lRZA_My9iS1BNRomKHP_mE0hFe5uFNOGP3D4DT2E#provenance http://rdf.disgenet.org/resource/nanopub/NP1010927.RAq0_lRZA_My9iS1BNRomKHP_mE0hFe5uFNOGP3D4DT2E#assertion http://purl.org/dc/terms/description [By contrast, the frequencies of the common H63D mutation did not differ, and the allele frequencies of the less frequently observed sequence deviations as substitution S65C in the HFE gene and mutation Y250X in the TFR2 gene underlying hemochromatosis type 3 (HFE3) were < 0.02 both in PCT patients and controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP1010927.RAq0_lRZA_My9iS1BNRomKHP_mE0hFe5uFNOGP3D4DT2E#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/NP1010927.RAq0_lRZA_My9iS1BNRomKHP_mE0hFe5uFNOGP3D4DT2E#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/17298224 http://rdf.disgenet.org/resource/nanopub/NP1010927.RAq0_lRZA_My9iS1BNRomKHP_mE0hFe5uFNOGP3D4DT2E#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP1010927.RAq0_lRZA_My9iS1BNRomKHP_mE0hFe5uFNOGP3D4DT2E#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/NP1010927.RAq0_lRZA_My9iS1BNRomKHP_mE0hFe5uFNOGP3D4DT2E#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP1010927.RAq0_lRZA_My9iS1BNRomKHP_mE0hFe5uFNOGP3D4DT2E http://purl.org/dc/terms/created 2017-10-17T13:16:38+02:00 http://rdf.disgenet.org/resource/nanopub/NP1010927.RAq0_lRZA_My9iS1BNRomKHP_mE0hFe5uFNOGP3D4DT2E http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP1010927.RAq0_lRZA_My9iS1BNRomKHP_mE0hFe5uFNOGP3D4DT2E http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP1010927.RAq0_lRZA_My9iS1BNRomKHP_mE0hFe5uFNOGP3D4DT2E http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP1010927.RAq0_lRZA_My9iS1BNRomKHP_mE0hFe5uFNOGP3D4DT2E http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP1010927.RAq0_lRZA_My9iS1BNRomKHP_mE0hFe5uFNOGP3D4DT2E http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP1010927.RAq0_lRZA_My9iS1BNRomKHP_mE0hFe5uFNOGP3D4DT2E http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP1010927.RAq0_lRZA_My9iS1BNRomKHP_mE0hFe5uFNOGP3D4DT2E http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP1010927.RAq0_lRZA_My9iS1BNRomKHP_mE0hFe5uFNOGP3D4DT2E http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP1010927.RAq0_lRZA_My9iS1BNRomKHP_mE0hFe5uFNOGP3D4DT2E http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP1010927.RAq0_lRZA_My9iS1BNRomKHP_mE0hFe5uFNOGP3D4DT2E http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP1010927.RAq0_lRZA_My9iS1BNRomKHP_mE0hFe5uFNOGP3D4DT2E 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