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- source_evidence_literature type ECO_0000212 NP500712.RACZ67edNRO-DHIWsQw5ApLykvMe8HqJ_MKwvo-Mi2PfU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP500712.RACZ67edNRO-DHIWsQw5ApLykvMe8HqJ_MKwvo-Mi2PfU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP500712.RACZ67edNRO-DHIWsQw5ApLykvMe8HqJ_MKwvo-Mi2PfU130_provenance.
- NP500712.RACZ67edNRO-DHIWsQw5ApLykvMe8HqJ_MKwvo-Mi2PfU130_assertion description "[In humans, this could explain that low levels of hepcidin found during juvenile haemochromatosis and HFE-1 genetic haemochromatosis are associated with an iron overload phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP500712.RACZ67edNRO-DHIWsQw5ApLykvMe8HqJ_MKwvo-Mi2PfU130_provenance.
- NP500712.RACZ67edNRO-DHIWsQw5ApLykvMe8HqJ_MKwvo-Mi2PfU130_assertion evidence source_evidence_literature NP500712.RACZ67edNRO-DHIWsQw5ApLykvMe8HqJ_MKwvo-Mi2PfU130_provenance.
- NP500712.RACZ67edNRO-DHIWsQw5ApLykvMe8HqJ_MKwvo-Mi2PfU130_assertion SIO_000772 15974953 NP500712.RACZ67edNRO-DHIWsQw5ApLykvMe8HqJ_MKwvo-Mi2PfU130_provenance.
- NP500712.RACZ67edNRO-DHIWsQw5ApLykvMe8HqJ_MKwvo-Mi2PfU130_assertion wasDerivedFrom befree-2016 NP500712.RACZ67edNRO-DHIWsQw5ApLykvMe8HqJ_MKwvo-Mi2PfU130_provenance.
- NP500712.RACZ67edNRO-DHIWsQw5ApLykvMe8HqJ_MKwvo-Mi2PfU130_assertion wasGeneratedBy ECO_0000203 NP500712.RACZ67edNRO-DHIWsQw5ApLykvMe8HqJ_MKwvo-Mi2PfU130_provenance.
- befree-2016 importedOn "2016-02-19" NP500712.RACZ67edNRO-DHIWsQw5ApLykvMe8HqJ_MKwvo-Mi2PfU130_provenance.