Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP632478.RAIWKi_uH4iVfhi_YL4jGpJ56wFfRlQlmoQHQXBymVCYI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP632478.RAIWKi_uH4iVfhi_YL4jGpJ56wFfRlQlmoQHQXBymVCYI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP632478.RAIWKi_uH4iVfhi_YL4jGpJ56wFfRlQlmoQHQXBymVCYI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP632478.RAIWKi_uH4iVfhi_YL4jGpJ56wFfRlQlmoQHQXBymVCYI130_provenance.
- NP632478.RAIWKi_uH4iVfhi_YL4jGpJ56wFfRlQlmoQHQXBymVCYI130_assertion description "[Hereditary hemochromatosis (HH) is a genetic disease associated with iron overload, in which individuals homozygous for the mutant C282Y HFE associated allele are at risk of developing liver disease, diabetes and arthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP632478.RAIWKi_uH4iVfhi_YL4jGpJ56wFfRlQlmoQHQXBymVCYI130_provenance.
- NP632478.RAIWKi_uH4iVfhi_YL4jGpJ56wFfRlQlmoQHQXBymVCYI130_assertion evidence source_evidence_literature NP632478.RAIWKi_uH4iVfhi_YL4jGpJ56wFfRlQlmoQHQXBymVCYI130_provenance.
- NP632478.RAIWKi_uH4iVfhi_YL4jGpJ56wFfRlQlmoQHQXBymVCYI130_assertion SIO_000772 17904763 NP632478.RAIWKi_uH4iVfhi_YL4jGpJ56wFfRlQlmoQHQXBymVCYI130_provenance.
- NP632478.RAIWKi_uH4iVfhi_YL4jGpJ56wFfRlQlmoQHQXBymVCYI130_assertion wasDerivedFrom befree-2016 NP632478.RAIWKi_uH4iVfhi_YL4jGpJ56wFfRlQlmoQHQXBymVCYI130_provenance.
- NP632478.RAIWKi_uH4iVfhi_YL4jGpJ56wFfRlQlmoQHQXBymVCYI130_assertion wasGeneratedBy ECO_0000203 NP632478.RAIWKi_uH4iVfhi_YL4jGpJ56wFfRlQlmoQHQXBymVCYI130_provenance.
- befree-2016 importedOn "2016-02-19" NP632478.RAIWKi_uH4iVfhi_YL4jGpJ56wFfRlQlmoQHQXBymVCYI130_provenance.