Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP559895.RAY1ikst-HR8bEi7BKhsjTPbOOVkbsL8DTOUkTk41A_Yw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP559895.RAY1ikst-HR8bEi7BKhsjTPbOOVkbsL8DTOUkTk41A_Yw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP559895.RAY1ikst-HR8bEi7BKhsjTPbOOVkbsL8DTOUkTk41A_Yw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP559895.RAY1ikst-HR8bEi7BKhsjTPbOOVkbsL8DTOUkTk41A_Yw130_provenance.
- NP559895.RAY1ikst-HR8bEi7BKhsjTPbOOVkbsL8DTOUkTk41A_Yw130_assertion description "[In this study, we aimed to determine the frequency of polymorphisms in two DNA repair enzyme genes, xeroderma pigmentosum complementation group (XPD) codon 312 and X-ray complementing group1 (XRCC1) codon 399, in a sample of 208 cataract patients (69 with cortical, 69 with nuclear and 70 with posterior sub capsular) and 151 sex and age matched healthy controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP559895.RAY1ikst-HR8bEi7BKhsjTPbOOVkbsL8DTOUkTk41A_Yw130_provenance.
- NP559895.RAY1ikst-HR8bEi7BKhsjTPbOOVkbsL8DTOUkTk41A_Yw130_assertion evidence source_evidence_literature NP559895.RAY1ikst-HR8bEi7BKhsjTPbOOVkbsL8DTOUkTk41A_Yw130_provenance.
- NP559895.RAY1ikst-HR8bEi7BKhsjTPbOOVkbsL8DTOUkTk41A_Yw130_assertion SIO_000772 21245954 NP559895.RAY1ikst-HR8bEi7BKhsjTPbOOVkbsL8DTOUkTk41A_Yw130_provenance.
- NP559895.RAY1ikst-HR8bEi7BKhsjTPbOOVkbsL8DTOUkTk41A_Yw130_assertion wasDerivedFrom befree-20140225 NP559895.RAY1ikst-HR8bEi7BKhsjTPbOOVkbsL8DTOUkTk41A_Yw130_provenance.
- NP559895.RAY1ikst-HR8bEi7BKhsjTPbOOVkbsL8DTOUkTk41A_Yw130_assertion wasGeneratedBy ECO_0000203 NP559895.RAY1ikst-HR8bEi7BKhsjTPbOOVkbsL8DTOUkTk41A_Yw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP559895.RAY1ikst-HR8bEi7BKhsjTPbOOVkbsL8DTOUkTk41A_Yw130_provenance.