Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP668634.RAkRg-3L62ZMMe9H3Ynd2-0LPXbER5b1xx6tDTr590goM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP668634.RAkRg-3L62ZMMe9H3Ynd2-0LPXbER5b1xx6tDTr590goM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP668634.RAkRg-3L62ZMMe9H3Ynd2-0LPXbER5b1xx6tDTr590goM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP668634.RAkRg-3L62ZMMe9H3Ynd2-0LPXbER5b1xx6tDTr590goM130_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.
- NP668634.RAkRg-3L62ZMMe9H3Ynd2-0LPXbER5b1xx6tDTr590goM130_assertion evidence source_evidence_literature NP668634.RAkRg-3L62ZMMe9H3Ynd2-0LPXbER5b1xx6tDTr590goM130_provenance.
- NP668634.RAkRg-3L62ZMMe9H3Ynd2-0LPXbER5b1xx6tDTr590goM130_assertion SIO_000772 18447718 NP668634.RAkRg-3L62ZMMe9H3Ynd2-0LPXbER5b1xx6tDTr590goM130_provenance.
- NP668634.RAkRg-3L62ZMMe9H3Ynd2-0LPXbER5b1xx6tDTr590goM130_assertion wasDerivedFrom befree-2016 NP668634.RAkRg-3L62ZMMe9H3Ynd2-0LPXbER5b1xx6tDTr590goM130_provenance.
- NP668634.RAkRg-3L62ZMMe9H3Ynd2-0LPXbER5b1xx6tDTr590goM130_assertion wasGeneratedBy ECO_0000203 NP668634.RAkRg-3L62ZMMe9H3Ynd2-0LPXbER5b1xx6tDTr590goM130_provenance.
- befree-2016 importedOn "2016-02-19" NP668634.RAkRg-3L62ZMMe9H3Ynd2-0LPXbER5b1xx6tDTr590goM130_provenance.