Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP385965.RAYiEEYYdY830MNnVhbFVNKCl-QeP5VHT3MP6ajaxC0rg130_assertion> ?p ?o ?g. }
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- NP385965.RAYiEEYYdY830MNnVhbFVNKCl-QeP5VHT3MP6ajaxC0rg130_assertion type Assertion NP385965.RAYiEEYYdY830MNnVhbFVNKCl-QeP5VHT3MP6ajaxC0rg130_head.
- NP385965.RAYiEEYYdY830MNnVhbFVNKCl-QeP5VHT3MP6ajaxC0rg130_assertion wasGeneratedBy ECO_0000203 NP385965.RAYiEEYYdY830MNnVhbFVNKCl-QeP5VHT3MP6ajaxC0rg130_provenance.
- NP385965.RAYiEEYYdY830MNnVhbFVNKCl-QeP5VHT3MP6ajaxC0rg130_assertion wasDerivedFrom befree-2016 NP385965.RAYiEEYYdY830MNnVhbFVNKCl-QeP5VHT3MP6ajaxC0rg130_provenance.
- NP385965.RAYiEEYYdY830MNnVhbFVNKCl-QeP5VHT3MP6ajaxC0rg130_assertion SIO_000772 12620480 NP385965.RAYiEEYYdY830MNnVhbFVNKCl-QeP5VHT3MP6ajaxC0rg130_provenance.
- NP385965.RAYiEEYYdY830MNnVhbFVNKCl-QeP5VHT3MP6ajaxC0rg130_assertion evidence source_evidence_literature NP385965.RAYiEEYYdY830MNnVhbFVNKCl-QeP5VHT3MP6ajaxC0rg130_provenance.
- NP385965.RAYiEEYYdY830MNnVhbFVNKCl-QeP5VHT3MP6ajaxC0rg130_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." NP385965.RAYiEEYYdY830MNnVhbFVNKCl-QeP5VHT3MP6ajaxC0rg130_provenance.