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- source_evidence_literature type ECO_0000212 NP92611.RA6U85ErJM7DWGyK3Tl35hB-d0WIdJVr_hXP17ooX95nA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP92611.RA6U85ErJM7DWGyK3Tl35hB-d0WIdJVr_hXP17ooX95nA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP92611.RA6U85ErJM7DWGyK3Tl35hB-d0WIdJVr_hXP17ooX95nA130_provenance.
- NP92611.RA6U85ErJM7DWGyK3Tl35hB-d0WIdJVr_hXP17ooX95nA130_assertion description "[, our data provide evidence that support the association between the MTR A2756G and MTRR G66A polymorphisms and SCCHN risk and that these two polymorphisms may have a joint effect on risk of SCCHN.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92611.RA6U85ErJM7DWGyK3Tl35hB-d0WIdJVr_hXP17ooX95nA130_provenance.
- NP92611.RA6U85ErJM7DWGyK3Tl35hB-d0WIdJVr_hXP17ooX95nA130_assertion evidence source_evidence_literature NP92611.RA6U85ErJM7DWGyK3Tl35hB-d0WIdJVr_hXP17ooX95nA130_provenance.
- NP92611.RA6U85ErJM7DWGyK3Tl35hB-d0WIdJVr_hXP17ooX95nA130_assertion SIO_000772 15894670 NP92611.RA6U85ErJM7DWGyK3Tl35hB-d0WIdJVr_hXP17ooX95nA130_provenance.
- NP92611.RA6U85ErJM7DWGyK3Tl35hB-d0WIdJVr_hXP17ooX95nA130_assertion wasDerivedFrom gad-20150221 NP92611.RA6U85ErJM7DWGyK3Tl35hB-d0WIdJVr_hXP17ooX95nA130_provenance.
- NP92611.RA6U85ErJM7DWGyK3Tl35hB-d0WIdJVr_hXP17ooX95nA130_assertion wasGeneratedBy ECO_0000203 NP92611.RA6U85ErJM7DWGyK3Tl35hB-d0WIdJVr_hXP17ooX95nA130_provenance.
- gad-20150221 importedOn "2015-02-21" NP92611.RA6U85ErJM7DWGyK3Tl35hB-d0WIdJVr_hXP17ooX95nA130_provenance.