Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP89875.RA3rgvWK7zaiIc-Xq2y3khjr6XUXipMw0OKtyR_KrQ7mY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP89875.RA3rgvWK7zaiIc-Xq2y3khjr6XUXipMw0OKtyR_KrQ7mY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP89875.RA3rgvWK7zaiIc-Xq2y3khjr6XUXipMw0OKtyR_KrQ7mY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP89875.RA3rgvWK7zaiIc-Xq2y3khjr6XUXipMw0OKtyR_KrQ7mY130_provenance.
- NP89875.RA3rgvWK7zaiIc-Xq2y3khjr6XUXipMw0OKtyR_KrQ7mY130_assertion description "[No association was observed between the GSTT1 gene deletion or the CYP1A1 m1, m2, and m3 polymorphisms with SIDS risk when considered independently or in combination.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89875.RA3rgvWK7zaiIc-Xq2y3khjr6XUXipMw0OKtyR_KrQ7mY130_provenance.
- NP89875.RA3rgvWK7zaiIc-Xq2y3khjr6XUXipMw0OKtyR_KrQ7mY130_assertion evidence source_evidence_literature NP89875.RA3rgvWK7zaiIc-Xq2y3khjr6XUXipMw0OKtyR_KrQ7mY130_provenance.
- NP89875.RA3rgvWK7zaiIc-Xq2y3khjr6XUXipMw0OKtyR_KrQ7mY130_assertion SIO_000772 16763966 NP89875.RA3rgvWK7zaiIc-Xq2y3khjr6XUXipMw0OKtyR_KrQ7mY130_provenance.
- NP89875.RA3rgvWK7zaiIc-Xq2y3khjr6XUXipMw0OKtyR_KrQ7mY130_assertion wasDerivedFrom gad-20130706 NP89875.RA3rgvWK7zaiIc-Xq2y3khjr6XUXipMw0OKtyR_KrQ7mY130_provenance.
- NP89875.RA3rgvWK7zaiIc-Xq2y3khjr6XUXipMw0OKtyR_KrQ7mY130_assertion wasGeneratedBy ECO_0000203 NP89875.RA3rgvWK7zaiIc-Xq2y3khjr6XUXipMw0OKtyR_KrQ7mY130_provenance.
- gad-20130706 importedOn "2013-07-06" NP89875.RA3rgvWK7zaiIc-Xq2y3khjr6XUXipMw0OKtyR_KrQ7mY130_provenance.