Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP167849.RAhnOZlXP1oRfQ_bvfIdFA2_EvHVfKOxSdb4bIrH1kZNk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP167849.RAhnOZlXP1oRfQ_bvfIdFA2_EvHVfKOxSdb4bIrH1kZNk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP167849.RAhnOZlXP1oRfQ_bvfIdFA2_EvHVfKOxSdb4bIrH1kZNk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP167849.RAhnOZlXP1oRfQ_bvfIdFA2_EvHVfKOxSdb4bIrH1kZNk130_provenance.
- NP167849.RAhnOZlXP1oRfQ_bvfIdFA2_EvHVfKOxSdb4bIrH1kZNk130_assertion description "[Single-nucleotide polymorphisms in the p53 pathway genes modify cancer risk in BRCA1 and BRCA2 carriers of Jewish-Ashkenazi descent.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP167849.RAhnOZlXP1oRfQ_bvfIdFA2_EvHVfKOxSdb4bIrH1kZNk130_provenance.
- NP167849.RAhnOZlXP1oRfQ_bvfIdFA2_EvHVfKOxSdb4bIrH1kZNk130_assertion evidence source_evidence_literature NP167849.RAhnOZlXP1oRfQ_bvfIdFA2_EvHVfKOxSdb4bIrH1kZNk130_provenance.
- NP167849.RAhnOZlXP1oRfQ_bvfIdFA2_EvHVfKOxSdb4bIrH1kZNk130_assertion SIO_000772 20306497 NP167849.RAhnOZlXP1oRfQ_bvfIdFA2_EvHVfKOxSdb4bIrH1kZNk130_provenance.
- NP167849.RAhnOZlXP1oRfQ_bvfIdFA2_EvHVfKOxSdb4bIrH1kZNk130_assertion wasDerivedFrom gad-20150221 NP167849.RAhnOZlXP1oRfQ_bvfIdFA2_EvHVfKOxSdb4bIrH1kZNk130_provenance.
- NP167849.RAhnOZlXP1oRfQ_bvfIdFA2_EvHVfKOxSdb4bIrH1kZNk130_assertion wasGeneratedBy ECO_0000203 NP167849.RAhnOZlXP1oRfQ_bvfIdFA2_EvHVfKOxSdb4bIrH1kZNk130_provenance.
- gad-20150221 importedOn "2015-02-21" NP167849.RAhnOZlXP1oRfQ_bvfIdFA2_EvHVfKOxSdb4bIrH1kZNk130_provenance.