Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP446701.RAgyZGGQToHnCMc_H4GxI07ykFpiwOiiyVFbCMjS5B7Vs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP446701.RAgyZGGQToHnCMc_H4GxI07ykFpiwOiiyVFbCMjS5B7Vs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP446701.RAgyZGGQToHnCMc_H4GxI07ykFpiwOiiyVFbCMjS5B7Vs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP446701.RAgyZGGQToHnCMc_H4GxI07ykFpiwOiiyVFbCMjS5B7Vs130_provenance.
- NP446701.RAgyZGGQToHnCMc_H4GxI07ykFpiwOiiyVFbCMjS5B7Vs130_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." NP446701.RAgyZGGQToHnCMc_H4GxI07ykFpiwOiiyVFbCMjS5B7Vs130_provenance.
- NP446701.RAgyZGGQToHnCMc_H4GxI07ykFpiwOiiyVFbCMjS5B7Vs130_assertion evidence source_evidence_literature NP446701.RAgyZGGQToHnCMc_H4GxI07ykFpiwOiiyVFbCMjS5B7Vs130_provenance.
- NP446701.RAgyZGGQToHnCMc_H4GxI07ykFpiwOiiyVFbCMjS5B7Vs130_assertion SIO_000772 17904763 NP446701.RAgyZGGQToHnCMc_H4GxI07ykFpiwOiiyVFbCMjS5B7Vs130_provenance.
- NP446701.RAgyZGGQToHnCMc_H4GxI07ykFpiwOiiyVFbCMjS5B7Vs130_assertion wasDerivedFrom befree-20150227 NP446701.RAgyZGGQToHnCMc_H4GxI07ykFpiwOiiyVFbCMjS5B7Vs130_provenance.
- NP446701.RAgyZGGQToHnCMc_H4GxI07ykFpiwOiiyVFbCMjS5B7Vs130_assertion wasGeneratedBy ECO_0000203 NP446701.RAgyZGGQToHnCMc_H4GxI07ykFpiwOiiyVFbCMjS5B7Vs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP446701.RAgyZGGQToHnCMc_H4GxI07ykFpiwOiiyVFbCMjS5B7Vs130_provenance.