Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP714850.RAP9PooVNORMLXhvM6OYoLtG0ijphsV8lAnuLtTCoPJFk130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP714850.RAP9PooVNORMLXhvM6OYoLtG0ijphsV8lAnuLtTCoPJFk130_assertion type Assertion NP714850.RAP9PooVNORMLXhvM6OYoLtG0ijphsV8lAnuLtTCoPJFk130_head.
- NP714850.RAP9PooVNORMLXhvM6OYoLtG0ijphsV8lAnuLtTCoPJFk130_assertion description "[Then, the type of liver siderosis (parenchymal, mesenchymal or mixed) and its distribution throughout the lobule and the liver are useful means for suggesting its etiology: HLA-linked hemochromatosis gene (HFE) hemochromatosis or other rare genetic hemochromatosis, nonhemochromatotic genetic iron overload (ferroportin disease, aceruloplasminemia), or iron overload secondary to excessive iron supply, inflammatory syndrome, noncirrhotic chronic liver diseases including dysmetabolic iron overload syndrome, cirrhosis, and blood disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP714850.RAP9PooVNORMLXhvM6OYoLtG0ijphsV8lAnuLtTCoPJFk130_provenance.
- NP714850.RAP9PooVNORMLXhvM6OYoLtG0ijphsV8lAnuLtTCoPJFk130_assertion evidence source_evidence_literature NP714850.RAP9PooVNORMLXhvM6OYoLtG0ijphsV8lAnuLtTCoPJFk130_provenance.
- NP714850.RAP9PooVNORMLXhvM6OYoLtG0ijphsV8lAnuLtTCoPJFk130_assertion SIO_000772 17729397 NP714850.RAP9PooVNORMLXhvM6OYoLtG0ijphsV8lAnuLtTCoPJFk130_provenance.
- NP714850.RAP9PooVNORMLXhvM6OYoLtG0ijphsV8lAnuLtTCoPJFk130_assertion wasDerivedFrom befree-20140225 NP714850.RAP9PooVNORMLXhvM6OYoLtG0ijphsV8lAnuLtTCoPJFk130_provenance.
- NP714850.RAP9PooVNORMLXhvM6OYoLtG0ijphsV8lAnuLtTCoPJFk130_assertion wasGeneratedBy ECO_0000203 NP714850.RAP9PooVNORMLXhvM6OYoLtG0ijphsV8lAnuLtTCoPJFk130_provenance.