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- source_evidence_literature type ECO_0000212 NP171811.RAqPbQzi4AfgPPiaz9z0CBlx6bky4j952eTRpG9uk6ITk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP171811.RAqPbQzi4AfgPPiaz9z0CBlx6bky4j952eTRpG9uk6ITk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP171811.RAqPbQzi4AfgPPiaz9z0CBlx6bky4j952eTRpG9uk6ITk130_provenance.
- NP171811.RAqPbQzi4AfgPPiaz9z0CBlx6bky4j952eTRpG9uk6ITk130_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." NP171811.RAqPbQzi4AfgPPiaz9z0CBlx6bky4j952eTRpG9uk6ITk130_provenance.
- NP171811.RAqPbQzi4AfgPPiaz9z0CBlx6bky4j952eTRpG9uk6ITk130_assertion evidence source_evidence_literature NP171811.RAqPbQzi4AfgPPiaz9z0CBlx6bky4j952eTRpG9uk6ITk130_provenance.
- NP171811.RAqPbQzi4AfgPPiaz9z0CBlx6bky4j952eTRpG9uk6ITk130_assertion SIO_000772 17729397 NP171811.RAqPbQzi4AfgPPiaz9z0CBlx6bky4j952eTRpG9uk6ITk130_provenance.
- NP171811.RAqPbQzi4AfgPPiaz9z0CBlx6bky4j952eTRpG9uk6ITk130_assertion wasDerivedFrom befree-20140225 NP171811.RAqPbQzi4AfgPPiaz9z0CBlx6bky4j952eTRpG9uk6ITk130_provenance.
- NP171811.RAqPbQzi4AfgPPiaz9z0CBlx6bky4j952eTRpG9uk6ITk130_assertion wasGeneratedBy ECO_0000203 NP171811.RAqPbQzi4AfgPPiaz9z0CBlx6bky4j952eTRpG9uk6ITk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP171811.RAqPbQzi4AfgPPiaz9z0CBlx6bky4j952eTRpG9uk6ITk130_provenance.