Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- 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." provenance.
- NP668631.RAsEb4EoJhjTVSmXK8IaTzPoDfzfn1KvSyW__kwHt2NQ4130_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." NP668631.RAsEb4EoJhjTVSmXK8IaTzPoDfzfn1KvSyW__kwHt2NQ4130_provenance.
- NP668632.RAqVW-SLJAbzMYz5gOk1G698Sq94Rs2UH3SxTTMYRB-Pw130_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." NP668632.RAqVW-SLJAbzMYz5gOk1G698Sq94Rs2UH3SxTTMYRB-Pw130_provenance.
- NP668634.RAkRg-3L62ZMMe9H3Ynd2-0LPXbER5b1xx6tDTr590goM130_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." NP668634.RAkRg-3L62ZMMe9H3Ynd2-0LPXbER5b1xx6tDTr590goM130_provenance.
- 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.
- NP668633.RA3Vky_Y2bscvNn8eT2PZK1ZHLuN_eyEbh09z-f1TsxKI130_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." NP668633.RA3Vky_Y2bscvNn8eT2PZK1ZHLuN_eyEbh09z-f1TsxKI130_provenance.