Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP936352.RA0dT6fSrXJ38hA8yF-D46hAESqzIws1VsABx_4ZskPFE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP936352.RA0dT6fSrXJ38hA8yF-D46hAESqzIws1VsABx_4ZskPFE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP936352.RA0dT6fSrXJ38hA8yF-D46hAESqzIws1VsABx_4ZskPFE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP936352.RA0dT6fSrXJ38hA8yF-D46hAESqzIws1VsABx_4ZskPFE130_provenance.
- befree-2016 importedOn "2016-02-19" NP936352.RA0dT6fSrXJ38hA8yF-D46hAESqzIws1VsABx_4ZskPFE130_provenance.
- NP936352.RA0dT6fSrXJ38hA8yF-D46hAESqzIws1VsABx_4ZskPFE130_assertion wasGeneratedBy ECO_0000203 NP936352.RA0dT6fSrXJ38hA8yF-D46hAESqzIws1VsABx_4ZskPFE130_provenance.
- NP936352.RA0dT6fSrXJ38hA8yF-D46hAESqzIws1VsABx_4ZskPFE130_assertion wasDerivedFrom befree-2016 NP936352.RA0dT6fSrXJ38hA8yF-D46hAESqzIws1VsABx_4ZskPFE130_provenance.
- NP936352.RA0dT6fSrXJ38hA8yF-D46hAESqzIws1VsABx_4ZskPFE130_assertion SIO_000772 22054067 NP936352.RA0dT6fSrXJ38hA8yF-D46hAESqzIws1VsABx_4ZskPFE130_provenance.
- NP936352.RA0dT6fSrXJ38hA8yF-D46hAESqzIws1VsABx_4ZskPFE130_assertion evidence source_evidence_literature NP936352.RA0dT6fSrXJ38hA8yF-D46hAESqzIws1VsABx_4ZskPFE130_provenance.
- NP936352.RA0dT6fSrXJ38hA8yF-D46hAESqzIws1VsABx_4ZskPFE130_assertion description "[Our findings suggest that genetic variability in members of the GST gene family may be associated with an increased susceptibility to RCC and its progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936352.RA0dT6fSrXJ38hA8yF-D46hAESqzIws1VsABx_4ZskPFE130_provenance.