Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP122432.RAIhP7hncW_QJ93OkxBO-h4lWRBZryu_DsQEbWUMrSbWg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP122432.RAIhP7hncW_QJ93OkxBO-h4lWRBZryu_DsQEbWUMrSbWg130_assertion type Assertion NP122432.RAIhP7hncW_QJ93OkxBO-h4lWRBZryu_DsQEbWUMrSbWg130_head.
- NP122432.RAIhP7hncW_QJ93OkxBO-h4lWRBZryu_DsQEbWUMrSbWg130_assertion description "[The variant CBS c.844_855ins68 -- that is, the allele carrying the insertion (ins or i) as opposed to the wild-type allele designated as deletion (del or d) -- was significantly overrepresented in meningioma patients (dd/ id/ii: 0.81/0.18/0.01) in comparison with the controls (dd/id/ii: 0.88/0.12/0; 2 df, chi-square 8.97, p = 0.011; multiple nominal regression with age and sex as covariables).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP122432.RAIhP7hncW_QJ93OkxBO-h4lWRBZryu_DsQEbWUMrSbWg130_provenance.
- NP122432.RAIhP7hncW_QJ93OkxBO-h4lWRBZryu_DsQEbWUMrSbWg130_assertion evidence source_evidence_literature NP122432.RAIhP7hncW_QJ93OkxBO-h4lWRBZryu_DsQEbWUMrSbWg130_provenance.
- NP122432.RAIhP7hncW_QJ93OkxBO-h4lWRBZryu_DsQEbWUMrSbWg130_assertion SIO_000772 18447718 NP122432.RAIhP7hncW_QJ93OkxBO-h4lWRBZryu_DsQEbWUMrSbWg130_provenance.
- NP122432.RAIhP7hncW_QJ93OkxBO-h4lWRBZryu_DsQEbWUMrSbWg130_assertion wasDerivedFrom gad-20150221 NP122432.RAIhP7hncW_QJ93OkxBO-h4lWRBZryu_DsQEbWUMrSbWg130_provenance.
- NP122432.RAIhP7hncW_QJ93OkxBO-h4lWRBZryu_DsQEbWUMrSbWg130_assertion wasGeneratedBy ECO_0000203 NP122432.RAIhP7hncW_QJ93OkxBO-h4lWRBZryu_DsQEbWUMrSbWg130_provenance.