Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP550797.RATLvLdFHFIPXMyT1zc_67_g_sEV2OSt8Vk8DdB3SsqIQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP550797.RATLvLdFHFIPXMyT1zc_67_g_sEV2OSt8Vk8DdB3SsqIQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP550797.RATLvLdFHFIPXMyT1zc_67_g_sEV2OSt8Vk8DdB3SsqIQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP550797.RATLvLdFHFIPXMyT1zc_67_g_sEV2OSt8Vk8DdB3SsqIQ130_provenance.
- NP550797.RATLvLdFHFIPXMyT1zc_67_g_sEV2OSt8Vk8DdB3SsqIQ130_assertion description "[However, none of these was found to affect the HDR activity of BARD1, suggesting that any increased cancer risk conferred by these mutations is not because of defects in this repair mechanism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP550797.RATLvLdFHFIPXMyT1zc_67_g_sEV2OSt8Vk8DdB3SsqIQ130_provenance.
- NP550797.RATLvLdFHFIPXMyT1zc_67_g_sEV2OSt8Vk8DdB3SsqIQ130_assertion evidence source_evidence_literature NP550797.RATLvLdFHFIPXMyT1zc_67_g_sEV2OSt8Vk8DdB3SsqIQ130_provenance.
- NP550797.RATLvLdFHFIPXMyT1zc_67_g_sEV2OSt8Vk8DdB3SsqIQ130_assertion SIO_000772 17848578 NP550797.RATLvLdFHFIPXMyT1zc_67_g_sEV2OSt8Vk8DdB3SsqIQ130_provenance.
- NP550797.RATLvLdFHFIPXMyT1zc_67_g_sEV2OSt8Vk8DdB3SsqIQ130_assertion wasDerivedFrom befree-20140225 NP550797.RATLvLdFHFIPXMyT1zc_67_g_sEV2OSt8Vk8DdB3SsqIQ130_provenance.
- NP550797.RATLvLdFHFIPXMyT1zc_67_g_sEV2OSt8Vk8DdB3SsqIQ130_assertion wasGeneratedBy ECO_0000203 NP550797.RATLvLdFHFIPXMyT1zc_67_g_sEV2OSt8Vk8DdB3SsqIQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP550797.RATLvLdFHFIPXMyT1zc_67_g_sEV2OSt8Vk8DdB3SsqIQ130_provenance.