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- source_evidence_literature type ECO_0000212 NP1056444.RAtV9nRLSv1vP4rM9q8WZH1DplwVhhbcmfoqg1je5bXXQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1056444.RAtV9nRLSv1vP4rM9q8WZH1DplwVhhbcmfoqg1je5bXXQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1056444.RAtV9nRLSv1vP4rM9q8WZH1DplwVhhbcmfoqg1je5bXXQ130_provenance.
- NP1056444.RAtV9nRLSv1vP4rM9q8WZH1DplwVhhbcmfoqg1je5bXXQ130_assertion description "[Our data extend the number of SNPs present in the promoter region that could play a regulatory role in COMT gene and suggest that the genetic polymorphisms rs 165656 and rs 4646310 exert a role in TMD susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1056444.RAtV9nRLSv1vP4rM9q8WZH1DplwVhhbcmfoqg1je5bXXQ130_provenance.
- NP1056444.RAtV9nRLSv1vP4rM9q8WZH1DplwVhhbcmfoqg1je5bXXQ130_assertion evidence source_evidence_literature NP1056444.RAtV9nRLSv1vP4rM9q8WZH1DplwVhhbcmfoqg1je5bXXQ130_provenance.
- NP1056444.RAtV9nRLSv1vP4rM9q8WZH1DplwVhhbcmfoqg1je5bXXQ130_assertion SIO_000772 23446089 NP1056444.RAtV9nRLSv1vP4rM9q8WZH1DplwVhhbcmfoqg1je5bXXQ130_provenance.
- NP1056444.RAtV9nRLSv1vP4rM9q8WZH1DplwVhhbcmfoqg1je5bXXQ130_assertion wasDerivedFrom befree-2016 NP1056444.RAtV9nRLSv1vP4rM9q8WZH1DplwVhhbcmfoqg1je5bXXQ130_provenance.
- NP1056444.RAtV9nRLSv1vP4rM9q8WZH1DplwVhhbcmfoqg1je5bXXQ130_assertion wasGeneratedBy ECO_0000203 NP1056444.RAtV9nRLSv1vP4rM9q8WZH1DplwVhhbcmfoqg1je5bXXQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1056444.RAtV9nRLSv1vP4rM9q8WZH1DplwVhhbcmfoqg1je5bXXQ130_provenance.