Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP128341.RAl6Ri0n5wMpXQF3OoepIxRYjBkUnVngUBysn4CFigLds130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP128341.RAl6Ri0n5wMpXQF3OoepIxRYjBkUnVngUBysn4CFigLds130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP128341.RAl6Ri0n5wMpXQF3OoepIxRYjBkUnVngUBysn4CFigLds130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP128341.RAl6Ri0n5wMpXQF3OoepIxRYjBkUnVngUBysn4CFigLds130_provenance.
- NP128341.RAl6Ri0n5wMpXQF3OoepIxRYjBkUnVngUBysn4CFigLds130_assertion description "[We have genotyped nine putative functional single-nucleotide polymorphisms (SNP) in genes involved in steroid hormone synthesis (SRD5A2, CYP19A1, HSB17B1, and HSD17B4) and DNA repair (XRCC2, XRCC3, BRCA2, and RAD52) using two Australian ovarian cancer case-control studies, comprising a total of 1,466 cases and 1,821 controls of Caucasian origin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP128341.RAl6Ri0n5wMpXQF3OoepIxRYjBkUnVngUBysn4CFigLds130_provenance.
- NP128341.RAl6Ri0n5wMpXQF3OoepIxRYjBkUnVngUBysn4CFigLds130_assertion evidence source_evidence_literature NP128341.RAl6Ri0n5wMpXQF3OoepIxRYjBkUnVngUBysn4CFigLds130_provenance.
- NP128341.RAl6Ri0n5wMpXQF3OoepIxRYjBkUnVngUBysn4CFigLds130_assertion SIO_000772 18086758 NP128341.RAl6Ri0n5wMpXQF3OoepIxRYjBkUnVngUBysn4CFigLds130_provenance.
- NP128341.RAl6Ri0n5wMpXQF3OoepIxRYjBkUnVngUBysn4CFigLds130_assertion wasDerivedFrom gad-20150221 NP128341.RAl6Ri0n5wMpXQF3OoepIxRYjBkUnVngUBysn4CFigLds130_provenance.
- NP128341.RAl6Ri0n5wMpXQF3OoepIxRYjBkUnVngUBysn4CFigLds130_assertion wasGeneratedBy ECO_0000203 NP128341.RAl6Ri0n5wMpXQF3OoepIxRYjBkUnVngUBysn4CFigLds130_provenance.
- gad-20150221 importedOn "2015-02-21" NP128341.RAl6Ri0n5wMpXQF3OoepIxRYjBkUnVngUBysn4CFigLds130_provenance.