Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP382217.RA0jzXaKWGepI1fRilSkU763QDWBuWu7bpIUsfg_-SMFs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP382217.RA0jzXaKWGepI1fRilSkU763QDWBuWu7bpIUsfg_-SMFs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP382217.RA0jzXaKWGepI1fRilSkU763QDWBuWu7bpIUsfg_-SMFs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP382217.RA0jzXaKWGepI1fRilSkU763QDWBuWu7bpIUsfg_-SMFs130_provenance.
- NP382217.RA0jzXaKWGepI1fRilSkU763QDWBuWu7bpIUsfg_-SMFs130_assertion description "[A significant association was found between the combined heterozygous of XRCC3 and homozygous variant of XPD gene and CRC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP382217.RA0jzXaKWGepI1fRilSkU763QDWBuWu7bpIUsfg_-SMFs130_provenance.
- NP382217.RA0jzXaKWGepI1fRilSkU763QDWBuWu7bpIUsfg_-SMFs130_assertion evidence source_evidence_literature NP382217.RA0jzXaKWGepI1fRilSkU763QDWBuWu7bpIUsfg_-SMFs130_provenance.
- NP382217.RA0jzXaKWGepI1fRilSkU763QDWBuWu7bpIUsfg_-SMFs130_assertion SIO_000772 24687779 NP382217.RA0jzXaKWGepI1fRilSkU763QDWBuWu7bpIUsfg_-SMFs130_provenance.
- NP382217.RA0jzXaKWGepI1fRilSkU763QDWBuWu7bpIUsfg_-SMFs130_assertion wasDerivedFrom befree-20150227 NP382217.RA0jzXaKWGepI1fRilSkU763QDWBuWu7bpIUsfg_-SMFs130_provenance.
- NP382217.RA0jzXaKWGepI1fRilSkU763QDWBuWu7bpIUsfg_-SMFs130_assertion wasGeneratedBy ECO_0000203 NP382217.RA0jzXaKWGepI1fRilSkU763QDWBuWu7bpIUsfg_-SMFs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP382217.RA0jzXaKWGepI1fRilSkU763QDWBuWu7bpIUsfg_-SMFs130_provenance.