Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP278313.RAtKZWP0nO29_AC4NS_d6xP8DeSlHSxjGhRzN-xNAJHI8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP278313.RAtKZWP0nO29_AC4NS_d6xP8DeSlHSxjGhRzN-xNAJHI8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP278313.RAtKZWP0nO29_AC4NS_d6xP8DeSlHSxjGhRzN-xNAJHI8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP278313.RAtKZWP0nO29_AC4NS_d6xP8DeSlHSxjGhRzN-xNAJHI8130_provenance.
- NP278313.RAtKZWP0nO29_AC4NS_d6xP8DeSlHSxjGhRzN-xNAJHI8130_assertion description "[After adjusting the effects of confounding factors, there was no significant association between NOS1 3'-UTR C276T genotypes and TD occurrence (p=0.758).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP278313.RAtKZWP0nO29_AC4NS_d6xP8DeSlHSxjGhRzN-xNAJHI8130_provenance.
- NP278313.RAtKZWP0nO29_AC4NS_d6xP8DeSlHSxjGhRzN-xNAJHI8130_assertion evidence source_evidence_literature NP278313.RAtKZWP0nO29_AC4NS_d6xP8DeSlHSxjGhRzN-xNAJHI8130_provenance.
- NP278313.RAtKZWP0nO29_AC4NS_d6xP8DeSlHSxjGhRzN-xNAJHI8130_assertion SIO_000772 15088155 NP278313.RAtKZWP0nO29_AC4NS_d6xP8DeSlHSxjGhRzN-xNAJHI8130_provenance.
- NP278313.RAtKZWP0nO29_AC4NS_d6xP8DeSlHSxjGhRzN-xNAJHI8130_assertion wasDerivedFrom befree-20140225 NP278313.RAtKZWP0nO29_AC4NS_d6xP8DeSlHSxjGhRzN-xNAJHI8130_provenance.
- NP278313.RAtKZWP0nO29_AC4NS_d6xP8DeSlHSxjGhRzN-xNAJHI8130_assertion wasGeneratedBy ECO_0000203 NP278313.RAtKZWP0nO29_AC4NS_d6xP8DeSlHSxjGhRzN-xNAJHI8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP278313.RAtKZWP0nO29_AC4NS_d6xP8DeSlHSxjGhRzN-xNAJHI8130_provenance.