Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP528628.RAJhTsydeFNbhbISQtwZGvM8GwW-lLCV-uhDWre_224YQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP528628.RAJhTsydeFNbhbISQtwZGvM8GwW-lLCV-uhDWre_224YQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP528628.RAJhTsydeFNbhbISQtwZGvM8GwW-lLCV-uhDWre_224YQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP528628.RAJhTsydeFNbhbISQtwZGvM8GwW-lLCV-uhDWre_224YQ130_provenance.
- NP528628.RAJhTsydeFNbhbISQtwZGvM8GwW-lLCV-uhDWre_224YQ130_assertion description "[Recent genome-wide scans identified several novel breast cancer risk alleles, including variants of the FGFR2, MAP3K1 and LSP1 genes, and a study of associations between these alleles and characteristics of breast cancer patients reported a borderline significant correlation between the number of FGFR2 minor alleles and family history of breast/ovarian cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP528628.RAJhTsydeFNbhbISQtwZGvM8GwW-lLCV-uhDWre_224YQ130_provenance.
- NP528628.RAJhTsydeFNbhbISQtwZGvM8GwW-lLCV-uhDWre_224YQ130_assertion evidence source_evidence_literature NP528628.RAJhTsydeFNbhbISQtwZGvM8GwW-lLCV-uhDWre_224YQ130_provenance.
- NP528628.RAJhTsydeFNbhbISQtwZGvM8GwW-lLCV-uhDWre_224YQ130_assertion SIO_000772 18973230 NP528628.RAJhTsydeFNbhbISQtwZGvM8GwW-lLCV-uhDWre_224YQ130_provenance.
- NP528628.RAJhTsydeFNbhbISQtwZGvM8GwW-lLCV-uhDWre_224YQ130_assertion wasDerivedFrom befree-20140225 NP528628.RAJhTsydeFNbhbISQtwZGvM8GwW-lLCV-uhDWre_224YQ130_provenance.
- NP528628.RAJhTsydeFNbhbISQtwZGvM8GwW-lLCV-uhDWre_224YQ130_assertion wasGeneratedBy ECO_0000203 NP528628.RAJhTsydeFNbhbISQtwZGvM8GwW-lLCV-uhDWre_224YQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP528628.RAJhTsydeFNbhbISQtwZGvM8GwW-lLCV-uhDWre_224YQ130_provenance.