Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP440917.RAQGNR9teWAaJlPKcc3lfBvJlG358cimHq7Dx6jhLIvSE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP440917.RAQGNR9teWAaJlPKcc3lfBvJlG358cimHq7Dx6jhLIvSE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP440917.RAQGNR9teWAaJlPKcc3lfBvJlG358cimHq7Dx6jhLIvSE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP440917.RAQGNR9teWAaJlPKcc3lfBvJlG358cimHq7Dx6jhLIvSE130_provenance.
- NP440917.RAQGNR9teWAaJlPKcc3lfBvJlG358cimHq7Dx6jhLIvSE130_assertion description "[Furthermore, a strong association was observed between the combination of GSTT1 null and GSTM1 null genotype and risk of BC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP440917.RAQGNR9teWAaJlPKcc3lfBvJlG358cimHq7Dx6jhLIvSE130_provenance.
- NP440917.RAQGNR9teWAaJlPKcc3lfBvJlG358cimHq7Dx6jhLIvSE130_assertion evidence source_evidence_literature NP440917.RAQGNR9teWAaJlPKcc3lfBvJlG358cimHq7Dx6jhLIvSE130_provenance.
- NP440917.RAQGNR9teWAaJlPKcc3lfBvJlG358cimHq7Dx6jhLIvSE130_assertion SIO_000772 22339266 NP440917.RAQGNR9teWAaJlPKcc3lfBvJlG358cimHq7Dx6jhLIvSE130_provenance.
- NP440917.RAQGNR9teWAaJlPKcc3lfBvJlG358cimHq7Dx6jhLIvSE130_assertion wasDerivedFrom befree-20150227 NP440917.RAQGNR9teWAaJlPKcc3lfBvJlG358cimHq7Dx6jhLIvSE130_provenance.
- NP440917.RAQGNR9teWAaJlPKcc3lfBvJlG358cimHq7Dx6jhLIvSE130_assertion wasGeneratedBy ECO_0000203 NP440917.RAQGNR9teWAaJlPKcc3lfBvJlG358cimHq7Dx6jhLIvSE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP440917.RAQGNR9teWAaJlPKcc3lfBvJlG358cimHq7Dx6jhLIvSE130_provenance.