Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP763797.RA0fAQAGlXlst_1XNyoqRolkVahORkPlyf8ZJ9q_t8e5o130_assertion> ?p ?o ?g. }
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- NP763797.RA0fAQAGlXlst_1XNyoqRolkVahORkPlyf8ZJ9q_t8e5o130_assertion type Assertion NP763797.RA0fAQAGlXlst_1XNyoqRolkVahORkPlyf8ZJ9q_t8e5o130_head.
- NP763797.RA0fAQAGlXlst_1XNyoqRolkVahORkPlyf8ZJ9q_t8e5o130_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." NP763797.RA0fAQAGlXlst_1XNyoqRolkVahORkPlyf8ZJ9q_t8e5o130_provenance.
- NP763797.RA0fAQAGlXlst_1XNyoqRolkVahORkPlyf8ZJ9q_t8e5o130_assertion evidence source_evidence_literature NP763797.RA0fAQAGlXlst_1XNyoqRolkVahORkPlyf8ZJ9q_t8e5o130_provenance.
- NP763797.RA0fAQAGlXlst_1XNyoqRolkVahORkPlyf8ZJ9q_t8e5o130_assertion SIO_000772 18447718 NP763797.RA0fAQAGlXlst_1XNyoqRolkVahORkPlyf8ZJ9q_t8e5o130_provenance.
- NP763797.RA0fAQAGlXlst_1XNyoqRolkVahORkPlyf8ZJ9q_t8e5o130_assertion wasDerivedFrom befree-20140225 NP763797.RA0fAQAGlXlst_1XNyoqRolkVahORkPlyf8ZJ9q_t8e5o130_provenance.
- NP763797.RA0fAQAGlXlst_1XNyoqRolkVahORkPlyf8ZJ9q_t8e5o130_assertion wasGeneratedBy ECO_0000203 NP763797.RA0fAQAGlXlst_1XNyoqRolkVahORkPlyf8ZJ9q_t8e5o130_provenance.