Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP327218.RApBIv7YRLJJatQuShq9nCVDAzxVumLnzjy-j0knOaR9Q130_assertion> ?p ?o ?g. }
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- NP327218.RApBIv7YRLJJatQuShq9nCVDAzxVumLnzjy-j0knOaR9Q130_assertion type Assertion NP327218.RApBIv7YRLJJatQuShq9nCVDAzxVumLnzjy-j0knOaR9Q130_head.
- NP327218.RApBIv7YRLJJatQuShq9nCVDAzxVumLnzjy-j0knOaR9Q130_assertion description "[A statistically significant (P=0.019) overrepresentation of C to G mutations within the NCCR Sp1 binding site was observed in 7/16 (43%) patients with HC (six cases at position 249 (P=0.035) and one case at position 251), as compared with 0/9 (0%) of the patients without HC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP327218.RApBIv7YRLJJatQuShq9nCVDAzxVumLnzjy-j0knOaR9Q130_provenance.
- NP327218.RApBIv7YRLJJatQuShq9nCVDAzxVumLnzjy-j0knOaR9Q130_assertion evidence source_evidence_literature NP327218.RApBIv7YRLJJatQuShq9nCVDAzxVumLnzjy-j0knOaR9Q130_provenance.
- NP327218.RApBIv7YRLJJatQuShq9nCVDAzxVumLnzjy-j0knOaR9Q130_assertion SIO_000772 11255092 NP327218.RApBIv7YRLJJatQuShq9nCVDAzxVumLnzjy-j0knOaR9Q130_provenance.
- NP327218.RApBIv7YRLJJatQuShq9nCVDAzxVumLnzjy-j0knOaR9Q130_assertion wasDerivedFrom befree-20140225 NP327218.RApBIv7YRLJJatQuShq9nCVDAzxVumLnzjy-j0knOaR9Q130_provenance.
- NP327218.RApBIv7YRLJJatQuShq9nCVDAzxVumLnzjy-j0knOaR9Q130_assertion wasGeneratedBy ECO_0000203 NP327218.RApBIv7YRLJJatQuShq9nCVDAzxVumLnzjy-j0knOaR9Q130_provenance.