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- source_evidence_literature type ECO_0000212 NP691279.RARZMpCwWQZ_F2ObxzZmQPtOvOwA6V3BAAJMkCJXNcqb8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP691279.RARZMpCwWQZ_F2ObxzZmQPtOvOwA6V3BAAJMkCJXNcqb8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP691279.RARZMpCwWQZ_F2ObxzZmQPtOvOwA6V3BAAJMkCJXNcqb8130_provenance.
- NP691279.RARZMpCwWQZ_F2ObxzZmQPtOvOwA6V3BAAJMkCJXNcqb8130_assertion description "[A significant positive association between the XRCC3 c.722 polymorphism and HNSCC was found, with an adjusted odds ratio (OR) of 1.96 (p=0.02).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP691279.RARZMpCwWQZ_F2ObxzZmQPtOvOwA6V3BAAJMkCJXNcqb8130_provenance.
- NP691279.RARZMpCwWQZ_F2ObxzZmQPtOvOwA6V3BAAJMkCJXNcqb8130_assertion evidence source_evidence_literature NP691279.RARZMpCwWQZ_F2ObxzZmQPtOvOwA6V3BAAJMkCJXNcqb8130_provenance.
- NP691279.RARZMpCwWQZ_F2ObxzZmQPtOvOwA6V3BAAJMkCJXNcqb8130_assertion SIO_000772 18768166 NP691279.RARZMpCwWQZ_F2ObxzZmQPtOvOwA6V3BAAJMkCJXNcqb8130_provenance.
- NP691279.RARZMpCwWQZ_F2ObxzZmQPtOvOwA6V3BAAJMkCJXNcqb8130_assertion wasDerivedFrom befree-2016 NP691279.RARZMpCwWQZ_F2ObxzZmQPtOvOwA6V3BAAJMkCJXNcqb8130_provenance.
- NP691279.RARZMpCwWQZ_F2ObxzZmQPtOvOwA6V3BAAJMkCJXNcqb8130_assertion wasGeneratedBy ECO_0000203 NP691279.RARZMpCwWQZ_F2ObxzZmQPtOvOwA6V3BAAJMkCJXNcqb8130_provenance.
- befree-2016 importedOn "2016-02-19" NP691279.RARZMpCwWQZ_F2ObxzZmQPtOvOwA6V3BAAJMkCJXNcqb8130_provenance.