Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP81408.RAp4rSUCLGxuHOElgW0-k1I5V0ScTL4_ULTRjUqdWVJiw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP81408.RAp4rSUCLGxuHOElgW0-k1I5V0ScTL4_ULTRjUqdWVJiw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP81408.RAp4rSUCLGxuHOElgW0-k1I5V0ScTL4_ULTRjUqdWVJiw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP81408.RAp4rSUCLGxuHOElgW0-k1I5V0ScTL4_ULTRjUqdWVJiw130_provenance.
- gad-20150221 importedOn "2015-02-21" NP81408.RAp4rSUCLGxuHOElgW0-k1I5V0ScTL4_ULTRjUqdWVJiw130_provenance.
- NP81408.RAp4rSUCLGxuHOElgW0-k1I5V0ScTL4_ULTRjUqdWVJiw130_assertion wasGeneratedBy ECO_0000203 NP81408.RAp4rSUCLGxuHOElgW0-k1I5V0ScTL4_ULTRjUqdWVJiw130_provenance.
- NP81408.RAp4rSUCLGxuHOElgW0-k1I5V0ScTL4_ULTRjUqdWVJiw130_assertion wasDerivedFrom gad-20150221 NP81408.RAp4rSUCLGxuHOElgW0-k1I5V0ScTL4_ULTRjUqdWVJiw130_provenance.
- NP81408.RAp4rSUCLGxuHOElgW0-k1I5V0ScTL4_ULTRjUqdWVJiw130_assertion SIO_000772 12620480 NP81408.RAp4rSUCLGxuHOElgW0-k1I5V0ScTL4_ULTRjUqdWVJiw130_provenance.
- NP81408.RAp4rSUCLGxuHOElgW0-k1I5V0ScTL4_ULTRjUqdWVJiw130_assertion evidence source_evidence_literature NP81408.RAp4rSUCLGxuHOElgW0-k1I5V0ScTL4_ULTRjUqdWVJiw130_provenance.
- NP81408.RAp4rSUCLGxuHOElgW0-k1I5V0ScTL4_ULTRjUqdWVJiw130_assertion description "[Our data suggest that CYP19 VNTR (TTTA)(10) allele as well as the combined genotype CYP1A1 m1 polymorphism and GSTM1 null deletion associate with the endometriosis phenotype, whereas the GSTT1 null deletion does not.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81408.RAp4rSUCLGxuHOElgW0-k1I5V0ScTL4_ULTRjUqdWVJiw130_provenance.