Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP677893.RAG8cPzPXz_rcWoFNcA1C4HjmlPCpowi8NtdkY2pRrLTg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP677893.RAG8cPzPXz_rcWoFNcA1C4HjmlPCpowi8NtdkY2pRrLTg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP677893.RAG8cPzPXz_rcWoFNcA1C4HjmlPCpowi8NtdkY2pRrLTg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP677893.RAG8cPzPXz_rcWoFNcA1C4HjmlPCpowi8NtdkY2pRrLTg130_provenance.
- NP677893.RAG8cPzPXz_rcWoFNcA1C4HjmlPCpowi8NtdkY2pRrLTg130_assertion description "[In subjects under age 60, for FASLG -844 C>T polymorphism, CT compared with the CC genotype, was significantly associated with increased risk of NSCLC, adjusted odds ratio (aOR) = 1.58 (1.22, 2.05), P = 0.0006 and TT aOR = 1.45 (1.01, 2.04), P = 0.04.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP677893.RAG8cPzPXz_rcWoFNcA1C4HjmlPCpowi8NtdkY2pRrLTg130_provenance.
- NP677893.RAG8cPzPXz_rcWoFNcA1C4HjmlPCpowi8NtdkY2pRrLTg130_assertion evidence source_evidence_literature NP677893.RAG8cPzPXz_rcWoFNcA1C4HjmlPCpowi8NtdkY2pRrLTg130_provenance.
- NP677893.RAG8cPzPXz_rcWoFNcA1C4HjmlPCpowi8NtdkY2pRrLTg130_assertion SIO_000772 18757527 NP677893.RAG8cPzPXz_rcWoFNcA1C4HjmlPCpowi8NtdkY2pRrLTg130_provenance.
- NP677893.RAG8cPzPXz_rcWoFNcA1C4HjmlPCpowi8NtdkY2pRrLTg130_assertion wasDerivedFrom befree-20140225 NP677893.RAG8cPzPXz_rcWoFNcA1C4HjmlPCpowi8NtdkY2pRrLTg130_provenance.
- NP677893.RAG8cPzPXz_rcWoFNcA1C4HjmlPCpowi8NtdkY2pRrLTg130_assertion wasGeneratedBy ECO_0000203 NP677893.RAG8cPzPXz_rcWoFNcA1C4HjmlPCpowi8NtdkY2pRrLTg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP677893.RAG8cPzPXz_rcWoFNcA1C4HjmlPCpowi8NtdkY2pRrLTg130_provenance.