Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP62783.RAAc5GI9Lrl-ChGRXaywKe_7Anb8pyv7pOCyawAXEkW_w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP62783.RAAc5GI9Lrl-ChGRXaywKe_7Anb8pyv7pOCyawAXEkW_w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP62783.RAAc5GI9Lrl-ChGRXaywKe_7Anb8pyv7pOCyawAXEkW_w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP62783.RAAc5GI9Lrl-ChGRXaywKe_7Anb8pyv7pOCyawAXEkW_w130_provenance.
- NP62783.RAAc5GI9Lrl-ChGRXaywKe_7Anb8pyv7pOCyawAXEkW_w130_assertion wasGeneratedBy ECO_0000203 NP62783.RAAc5GI9Lrl-ChGRXaywKe_7Anb8pyv7pOCyawAXEkW_w130_provenance.
- NP62783.RAAc5GI9Lrl-ChGRXaywKe_7Anb8pyv7pOCyawAXEkW_w130_assertion wasDerivedFrom gad-20130706 NP62783.RAAc5GI9Lrl-ChGRXaywKe_7Anb8pyv7pOCyawAXEkW_w130_provenance.
- NP62783.RAAc5GI9Lrl-ChGRXaywKe_7Anb8pyv7pOCyawAXEkW_w130_assertion SIO_000772 12620480 NP62783.RAAc5GI9Lrl-ChGRXaywKe_7Anb8pyv7pOCyawAXEkW_w130_provenance.
- NP62783.RAAc5GI9Lrl-ChGRXaywKe_7Anb8pyv7pOCyawAXEkW_w130_assertion evidence source_evidence_literature NP62783.RAAc5GI9Lrl-ChGRXaywKe_7Anb8pyv7pOCyawAXEkW_w130_provenance.
- NP62783.RAAc5GI9Lrl-ChGRXaywKe_7Anb8pyv7pOCyawAXEkW_w130_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." NP62783.RAAc5GI9Lrl-ChGRXaywKe_7Anb8pyv7pOCyawAXEkW_w130_provenance.
- gad-20130706 importedOn "2013-07-06" NP62783.RAAc5GI9Lrl-ChGRXaywKe_7Anb8pyv7pOCyawAXEkW_w130_provenance.