Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP813784.RAdH3vBzJssaYIGBY5zPUKr01tXQCw-a1yPBe2QcbIo0A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP813784.RAdH3vBzJssaYIGBY5zPUKr01tXQCw-a1yPBe2QcbIo0A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP813784.RAdH3vBzJssaYIGBY5zPUKr01tXQCw-a1yPBe2QcbIo0A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP813784.RAdH3vBzJssaYIGBY5zPUKr01tXQCw-a1yPBe2QcbIo0A130_provenance.
- NP813784.RAdH3vBzJssaYIGBY5zPUKr01tXQCw-a1yPBe2QcbIo0A130_assertion description "[There was a significantly higher frequency of coinheritance of the hereditary hemochromatosis (HH) HFE mutant allele C282Y in 18 unrelated XLSA hemizygotes than found in the normal population, indicating a role for coinheritance of HFE alleles in the expression of this disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP813784.RAdH3vBzJssaYIGBY5zPUKr01tXQCw-a1yPBe2QcbIo0A130_provenance.
- NP813784.RAdH3vBzJssaYIGBY5zPUKr01tXQCw-a1yPBe2QcbIo0A130_assertion evidence source_evidence_literature NP813784.RAdH3vBzJssaYIGBY5zPUKr01tXQCw-a1yPBe2QcbIo0A130_provenance.
- NP813784.RAdH3vBzJssaYIGBY5zPUKr01tXQCw-a1yPBe2QcbIo0A130_assertion SIO_000772 10029606 NP813784.RAdH3vBzJssaYIGBY5zPUKr01tXQCw-a1yPBe2QcbIo0A130_provenance.
- NP813784.RAdH3vBzJssaYIGBY5zPUKr01tXQCw-a1yPBe2QcbIo0A130_assertion wasDerivedFrom befree-20140225 NP813784.RAdH3vBzJssaYIGBY5zPUKr01tXQCw-a1yPBe2QcbIo0A130_provenance.
- NP813784.RAdH3vBzJssaYIGBY5zPUKr01tXQCw-a1yPBe2QcbIo0A130_assertion wasGeneratedBy ECO_0000203 NP813784.RAdH3vBzJssaYIGBY5zPUKr01tXQCw-a1yPBe2QcbIo0A130_provenance.
- befree-20140225 importedOn "2014-02-25" NP813784.RAdH3vBzJssaYIGBY5zPUKr01tXQCw-a1yPBe2QcbIo0A130_provenance.