Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP62783.RAAc5GI9Lrl-ChGRXaywKe_7Anb8pyv7pOCyawAXEkW_w130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP62783.RAAc5GI9Lrl-ChGRXaywKe_7Anb8pyv7pOCyawAXEkW_w130_assertion type Assertion NP62783.RAAc5GI9Lrl-ChGRXaywKe_7Anb8pyv7pOCyawAXEkW_w130_head.
- 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.