Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP627378.RAssrCc1PjfX5pTkjupyFKHxy5GxjVAwAWqXBR4bTkces130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP627378.RAssrCc1PjfX5pTkjupyFKHxy5GxjVAwAWqXBR4bTkces130_assertion type Assertion NP627378.RAssrCc1PjfX5pTkjupyFKHxy5GxjVAwAWqXBR4bTkces130_head.
- NP627378.RAssrCc1PjfX5pTkjupyFKHxy5GxjVAwAWqXBR4bTkces130_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." NP627378.RAssrCc1PjfX5pTkjupyFKHxy5GxjVAwAWqXBR4bTkces130_provenance.
- NP627378.RAssrCc1PjfX5pTkjupyFKHxy5GxjVAwAWqXBR4bTkces130_assertion evidence source_evidence_literature NP627378.RAssrCc1PjfX5pTkjupyFKHxy5GxjVAwAWqXBR4bTkces130_provenance.
- NP627378.RAssrCc1PjfX5pTkjupyFKHxy5GxjVAwAWqXBR4bTkces130_assertion SIO_000772 17729397 NP627378.RAssrCc1PjfX5pTkjupyFKHxy5GxjVAwAWqXBR4bTkces130_provenance.
- NP627378.RAssrCc1PjfX5pTkjupyFKHxy5GxjVAwAWqXBR4bTkces130_assertion wasDerivedFrom befree-2016 NP627378.RAssrCc1PjfX5pTkjupyFKHxy5GxjVAwAWqXBR4bTkces130_provenance.
- NP627378.RAssrCc1PjfX5pTkjupyFKHxy5GxjVAwAWqXBR4bTkces130_assertion wasGeneratedBy ECO_0000203 NP627378.RAssrCc1PjfX5pTkjupyFKHxy5GxjVAwAWqXBR4bTkces130_provenance.