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- source_evidence_literature type ECO_0000212 NP971578.RAvtju6iZf-Eu2STceSuCFFUQWnPxTrnnMIHNOlEEANpw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP971578.RAvtju6iZf-Eu2STceSuCFFUQWnPxTrnnMIHNOlEEANpw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP971578.RAvtju6iZf-Eu2STceSuCFFUQWnPxTrnnMIHNOlEEANpw130_provenance.
- NP971578.RAvtju6iZf-Eu2STceSuCFFUQWnPxTrnnMIHNOlEEANpw130_assertion description "[Our identification of XRCC2 as a breast cancer susceptibility gene thus increases the proportion of breast cancers that are associated with homologous recombination-DNA-repair dysfunction and Fanconi anemia and could therefore benefit from specific targeted treatments such as PARP (poly ADP ribose polymerase) inhibitors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP971578.RAvtju6iZf-Eu2STceSuCFFUQWnPxTrnnMIHNOlEEANpw130_provenance.
- NP971578.RAvtju6iZf-Eu2STceSuCFFUQWnPxTrnnMIHNOlEEANpw130_assertion evidence source_evidence_literature NP971578.RAvtju6iZf-Eu2STceSuCFFUQWnPxTrnnMIHNOlEEANpw130_provenance.
- NP971578.RAvtju6iZf-Eu2STceSuCFFUQWnPxTrnnMIHNOlEEANpw130_assertion SIO_000772 22464251 NP971578.RAvtju6iZf-Eu2STceSuCFFUQWnPxTrnnMIHNOlEEANpw130_provenance.
- NP971578.RAvtju6iZf-Eu2STceSuCFFUQWnPxTrnnMIHNOlEEANpw130_assertion wasDerivedFrom befree-2016 NP971578.RAvtju6iZf-Eu2STceSuCFFUQWnPxTrnnMIHNOlEEANpw130_provenance.
- NP971578.RAvtju6iZf-Eu2STceSuCFFUQWnPxTrnnMIHNOlEEANpw130_assertion wasGeneratedBy ECO_0000203 NP971578.RAvtju6iZf-Eu2STceSuCFFUQWnPxTrnnMIHNOlEEANpw130_provenance.
- befree-2016 importedOn "2016-02-19" NP971578.RAvtju6iZf-Eu2STceSuCFFUQWnPxTrnnMIHNOlEEANpw130_provenance.