Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1175824.RAcXaE7let7k3WOmtnXMv6mqYlL-MWRPSx3WMDF7i0Qv4130_assertion> ?p ?o ?g. }
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- NP1175824.RAcXaE7let7k3WOmtnXMv6mqYlL-MWRPSx3WMDF7i0Qv4130_assertion type Assertion NP1175824.RAcXaE7let7k3WOmtnXMv6mqYlL-MWRPSx3WMDF7i0Qv4130_head.
- NP1175824.RAcXaE7let7k3WOmtnXMv6mqYlL-MWRPSx3WMDF7i0Qv4130_assertion description "[The variant 'A' allele in MLLT10 rs12770228 was associated with an increased risk of meningioma (per allele odds ratio: 1.25; 95% confidence interval: 1.02, 1.53; P=0.031).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1175824.RAcXaE7let7k3WOmtnXMv6mqYlL-MWRPSx3WMDF7i0Qv4130_provenance.
- NP1175824.RAcXaE7let7k3WOmtnXMv6mqYlL-MWRPSx3WMDF7i0Qv4130_assertion evidence source_evidence_literature NP1175824.RAcXaE7let7k3WOmtnXMv6mqYlL-MWRPSx3WMDF7i0Qv4130_provenance.
- NP1175824.RAcXaE7let7k3WOmtnXMv6mqYlL-MWRPSx3WMDF7i0Qv4130_assertion SIO_000772 24755950 NP1175824.RAcXaE7let7k3WOmtnXMv6mqYlL-MWRPSx3WMDF7i0Qv4130_provenance.
- NP1175824.RAcXaE7let7k3WOmtnXMv6mqYlL-MWRPSx3WMDF7i0Qv4130_assertion wasDerivedFrom befree-2016 NP1175824.RAcXaE7let7k3WOmtnXMv6mqYlL-MWRPSx3WMDF7i0Qv4130_provenance.
- NP1175824.RAcXaE7let7k3WOmtnXMv6mqYlL-MWRPSx3WMDF7i0Qv4130_assertion wasGeneratedBy ECO_0000203 NP1175824.RAcXaE7let7k3WOmtnXMv6mqYlL-MWRPSx3WMDF7i0Qv4130_provenance.