Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP768753.RAuh1y6rnuSpqYvWC7uFNpEptzp7qg0mLjuMSIdtUDcDY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP768753.RAuh1y6rnuSpqYvWC7uFNpEptzp7qg0mLjuMSIdtUDcDY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP768753.RAuh1y6rnuSpqYvWC7uFNpEptzp7qg0mLjuMSIdtUDcDY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP768753.RAuh1y6rnuSpqYvWC7uFNpEptzp7qg0mLjuMSIdtUDcDY130_provenance.
- NP768753.RAuh1y6rnuSpqYvWC7uFNpEptzp7qg0mLjuMSIdtUDcDY130_assertion description "[None of the four cases with the HFE genotype associated with high risk of HH in the control groups presented iron overload; however, in eight of 11 subjects (72.7%) with primary HTG and HH genetic predisposition, the iron overload was present.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP768753.RAuh1y6rnuSpqYvWC7uFNpEptzp7qg0mLjuMSIdtUDcDY130_provenance.
- NP768753.RAuh1y6rnuSpqYvWC7uFNpEptzp7qg0mLjuMSIdtUDcDY130_assertion evidence source_evidence_literature NP768753.RAuh1y6rnuSpqYvWC7uFNpEptzp7qg0mLjuMSIdtUDcDY130_provenance.
- NP768753.RAuh1y6rnuSpqYvWC7uFNpEptzp7qg0mLjuMSIdtUDcDY130_assertion SIO_000772 19820015 NP768753.RAuh1y6rnuSpqYvWC7uFNpEptzp7qg0mLjuMSIdtUDcDY130_provenance.
- NP768753.RAuh1y6rnuSpqYvWC7uFNpEptzp7qg0mLjuMSIdtUDcDY130_assertion wasDerivedFrom befree-2016 NP768753.RAuh1y6rnuSpqYvWC7uFNpEptzp7qg0mLjuMSIdtUDcDY130_provenance.
- NP768753.RAuh1y6rnuSpqYvWC7uFNpEptzp7qg0mLjuMSIdtUDcDY130_assertion wasGeneratedBy ECO_0000203 NP768753.RAuh1y6rnuSpqYvWC7uFNpEptzp7qg0mLjuMSIdtUDcDY130_provenance.
- befree-2016 importedOn "2016-02-19" NP768753.RAuh1y6rnuSpqYvWC7uFNpEptzp7qg0mLjuMSIdtUDcDY130_provenance.