Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP217773.RA-8s9zTb7sySy07jnEZkoQG0WodNHjKByIf6cahfEnOg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP217773.RA-8s9zTb7sySy07jnEZkoQG0WodNHjKByIf6cahfEnOg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP217773.RA-8s9zTb7sySy07jnEZkoQG0WodNHjKByIf6cahfEnOg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP217773.RA-8s9zTb7sySy07jnEZkoQG0WodNHjKByIf6cahfEnOg130_provenance.
- NP217773.RA-8s9zTb7sySy07jnEZkoQG0WodNHjKByIf6cahfEnOg130_assertion description "[The GSTT2B deletion was not associated with OSCC risk in the Black population, but was associated with reduced risk of OSCC in the Mixed Ancestry population (OR=0.71; 95% CI 0.57-0.90, p=0.004).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217773.RA-8s9zTb7sySy07jnEZkoQG0WodNHjKByIf6cahfEnOg130_provenance.
- NP217773.RA-8s9zTb7sySy07jnEZkoQG0WodNHjKByIf6cahfEnOg130_assertion evidence source_evidence_literature NP217773.RA-8s9zTb7sySy07jnEZkoQG0WodNHjKByIf6cahfEnOg130_provenance.
- NP217773.RA-8s9zTb7sySy07jnEZkoQG0WodNHjKByIf6cahfEnOg130_assertion SIO_000772 22216261 NP217773.RA-8s9zTb7sySy07jnEZkoQG0WodNHjKByIf6cahfEnOg130_provenance.
- NP217773.RA-8s9zTb7sySy07jnEZkoQG0WodNHjKByIf6cahfEnOg130_assertion wasDerivedFrom befree-20140225 NP217773.RA-8s9zTb7sySy07jnEZkoQG0WodNHjKByIf6cahfEnOg130_provenance.
- NP217773.RA-8s9zTb7sySy07jnEZkoQG0WodNHjKByIf6cahfEnOg130_assertion wasGeneratedBy ECO_0000203 NP217773.RA-8s9zTb7sySy07jnEZkoQG0WodNHjKByIf6cahfEnOg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP217773.RA-8s9zTb7sySy07jnEZkoQG0WodNHjKByIf6cahfEnOg130_provenance.