Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP933607.RAcKilNL1UAs2s1rm4k4nmCFsmQb-9ZCijtSpfXwos6W0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP933607.RAcKilNL1UAs2s1rm4k4nmCFsmQb-9ZCijtSpfXwos6W0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP933607.RAcKilNL1UAs2s1rm4k4nmCFsmQb-9ZCijtSpfXwos6W0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP933607.RAcKilNL1UAs2s1rm4k4nmCFsmQb-9ZCijtSpfXwos6W0130_provenance.
- NP933607.RAcKilNL1UAs2s1rm4k4nmCFsmQb-9ZCijtSpfXwos6W0130_assertion description "[In the present study, we examined gene expression of duodenal iron transport molecules and hepcidin in patients with hereditary hemochromatosis (HHC) (treated and untreated), involving various genotypes (genotypes which represent risk for HHC were examined), and in patients with iron deficiency anaemia (IDA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP933607.RAcKilNL1UAs2s1rm4k4nmCFsmQb-9ZCijtSpfXwos6W0130_provenance.
- NP933607.RAcKilNL1UAs2s1rm4k4nmCFsmQb-9ZCijtSpfXwos6W0130_assertion evidence source_evidence_literature NP933607.RAcKilNL1UAs2s1rm4k4nmCFsmQb-9ZCijtSpfXwos6W0130_provenance.
- NP933607.RAcKilNL1UAs2s1rm4k4nmCFsmQb-9ZCijtSpfXwos6W0130_assertion SIO_000772 21973163 NP933607.RAcKilNL1UAs2s1rm4k4nmCFsmQb-9ZCijtSpfXwos6W0130_provenance.
- NP933607.RAcKilNL1UAs2s1rm4k4nmCFsmQb-9ZCijtSpfXwos6W0130_assertion wasDerivedFrom befree-20150227 NP933607.RAcKilNL1UAs2s1rm4k4nmCFsmQb-9ZCijtSpfXwos6W0130_provenance.
- NP933607.RAcKilNL1UAs2s1rm4k4nmCFsmQb-9ZCijtSpfXwos6W0130_assertion wasGeneratedBy ECO_0000203 NP933607.RAcKilNL1UAs2s1rm4k4nmCFsmQb-9ZCijtSpfXwos6W0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP933607.RAcKilNL1UAs2s1rm4k4nmCFsmQb-9ZCijtSpfXwos6W0130_provenance.