Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP286866.RAxfG2nn_Vs1amcrYS3j8hKSx29FMmMI0pTLPMxzk-2Fs130_assertion> ?p ?o ?g. }
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- NP286866.RAxfG2nn_Vs1amcrYS3j8hKSx29FMmMI0pTLPMxzk-2Fs130_assertion type Assertion NP286866.RAxfG2nn_Vs1amcrYS3j8hKSx29FMmMI0pTLPMxzk-2Fs130_head.
- NP286866.RAxfG2nn_Vs1amcrYS3j8hKSx29FMmMI0pTLPMxzk-2Fs130_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." NP286866.RAxfG2nn_Vs1amcrYS3j8hKSx29FMmMI0pTLPMxzk-2Fs130_provenance.
- NP286866.RAxfG2nn_Vs1amcrYS3j8hKSx29FMmMI0pTLPMxzk-2Fs130_assertion evidence source_evidence_literature NP286866.RAxfG2nn_Vs1amcrYS3j8hKSx29FMmMI0pTLPMxzk-2Fs130_provenance.
- NP286866.RAxfG2nn_Vs1amcrYS3j8hKSx29FMmMI0pTLPMxzk-2Fs130_assertion SIO_000772 18447718 NP286866.RAxfG2nn_Vs1amcrYS3j8hKSx29FMmMI0pTLPMxzk-2Fs130_provenance.
- NP286866.RAxfG2nn_Vs1amcrYS3j8hKSx29FMmMI0pTLPMxzk-2Fs130_assertion wasDerivedFrom befree-20150227 NP286866.RAxfG2nn_Vs1amcrYS3j8hKSx29FMmMI0pTLPMxzk-2Fs130_provenance.
- NP286866.RAxfG2nn_Vs1amcrYS3j8hKSx29FMmMI0pTLPMxzk-2Fs130_assertion wasGeneratedBy ECO_0000203 NP286866.RAxfG2nn_Vs1amcrYS3j8hKSx29FMmMI0pTLPMxzk-2Fs130_provenance.