Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP752155.RAR9NNke_RVz4EHGGOBNeqw6lVfV0HD105HXegSRFoKcI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP752155.RAR9NNke_RVz4EHGGOBNeqw6lVfV0HD105HXegSRFoKcI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP752155.RAR9NNke_RVz4EHGGOBNeqw6lVfV0HD105HXegSRFoKcI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP752155.RAR9NNke_RVz4EHGGOBNeqw6lVfV0HD105HXegSRFoKcI130_provenance.
- NP752155.RAR9NNke_RVz4EHGGOBNeqw6lVfV0HD105HXegSRFoKcI130_assertion description "[Moreover, the detection of the TP53 R337H variant in our series and the fact that this variant has a founder effect in our population prompted us to suggest that all female breast cancer patients with clinical criteria for HBOC and negative for BRCA1/2 genes should be tested for the TP53 R337H variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP752155.RAR9NNke_RVz4EHGGOBNeqw6lVfV0HD105HXegSRFoKcI130_provenance.
- NP752155.RAR9NNke_RVz4EHGGOBNeqw6lVfV0HD105HXegSRFoKcI130_assertion evidence source_evidence_literature NP752155.RAR9NNke_RVz4EHGGOBNeqw6lVfV0HD105HXegSRFoKcI130_provenance.
- NP752155.RAR9NNke_RVz4EHGGOBNeqw6lVfV0HD105HXegSRFoKcI130_assertion SIO_000772 24884479 NP752155.RAR9NNke_RVz4EHGGOBNeqw6lVfV0HD105HXegSRFoKcI130_provenance.
- NP752155.RAR9NNke_RVz4EHGGOBNeqw6lVfV0HD105HXegSRFoKcI130_assertion wasDerivedFrom befree-20150227 NP752155.RAR9NNke_RVz4EHGGOBNeqw6lVfV0HD105HXegSRFoKcI130_provenance.
- NP752155.RAR9NNke_RVz4EHGGOBNeqw6lVfV0HD105HXegSRFoKcI130_assertion wasGeneratedBy ECO_0000203 NP752155.RAR9NNke_RVz4EHGGOBNeqw6lVfV0HD105HXegSRFoKcI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP752155.RAR9NNke_RVz4EHGGOBNeqw6lVfV0HD105HXegSRFoKcI130_provenance.