Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP70281.RA38LyzcW4xATaJ5dxn02NH3PPGKi3dqjfaw97hEwGUzI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP70281.RA38LyzcW4xATaJ5dxn02NH3PPGKi3dqjfaw97hEwGUzI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP70281.RA38LyzcW4xATaJ5dxn02NH3PPGKi3dqjfaw97hEwGUzI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP70281.RA38LyzcW4xATaJ5dxn02NH3PPGKi3dqjfaw97hEwGUzI130_provenance.
- NP70281.RA38LyzcW4xATaJ5dxn02NH3PPGKi3dqjfaw97hEwGUzI130_assertion description "[Polymorphisms in the LOXL1 gene confer risk to XFS/XFG in the Japanese, but there are different risk-associated alleles and haplotypes in the Japanese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP70281.RA38LyzcW4xATaJ5dxn02NH3PPGKi3dqjfaw97hEwGUzI130_provenance.
- NP70281.RA38LyzcW4xATaJ5dxn02NH3PPGKi3dqjfaw97hEwGUzI130_assertion evidence source_evidence_literature NP70281.RA38LyzcW4xATaJ5dxn02NH3PPGKi3dqjfaw97hEwGUzI130_provenance.
- NP70281.RA38LyzcW4xATaJ5dxn02NH3PPGKi3dqjfaw97hEwGUzI130_assertion SIO_000772 18450598 NP70281.RA38LyzcW4xATaJ5dxn02NH3PPGKi3dqjfaw97hEwGUzI130_provenance.
- NP70281.RA38LyzcW4xATaJ5dxn02NH3PPGKi3dqjfaw97hEwGUzI130_assertion wasDerivedFrom gad-20130706 NP70281.RA38LyzcW4xATaJ5dxn02NH3PPGKi3dqjfaw97hEwGUzI130_provenance.
- NP70281.RA38LyzcW4xATaJ5dxn02NH3PPGKi3dqjfaw97hEwGUzI130_assertion wasGeneratedBy ECO_0000203 NP70281.RA38LyzcW4xATaJ5dxn02NH3PPGKi3dqjfaw97hEwGUzI130_provenance.
- gad-20130706 importedOn "2013-07-06" NP70281.RA38LyzcW4xATaJ5dxn02NH3PPGKi3dqjfaw97hEwGUzI130_provenance.