Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1259648.RAGnB1NZ10kxCkiNeKuvnZQ_G8_O-8eQqUgi4gyRbONIA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1259648.RAGnB1NZ10kxCkiNeKuvnZQ_G8_O-8eQqUgi4gyRbONIA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1259648.RAGnB1NZ10kxCkiNeKuvnZQ_G8_O-8eQqUgi4gyRbONIA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1259648.RAGnB1NZ10kxCkiNeKuvnZQ_G8_O-8eQqUgi4gyRbONIA130_provenance.
- NP1259648.RAGnB1NZ10kxCkiNeKuvnZQ_G8_O-8eQqUgi4gyRbONIA130_assertion description "[There was a trend of reduced NPC risk in individuals who were homozygous for both HLA-E(?)01:03 and NKG2C deletion (0.46% vs. 2.51%, P=0.0076, Pcorrected=0.0684, OR (95% CI)=0.1794 (0.0473-0.6809)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1259648.RAGnB1NZ10kxCkiNeKuvnZQ_G8_O-8eQqUgi4gyRbONIA130_provenance.
- NP1259648.RAGnB1NZ10kxCkiNeKuvnZQ_G8_O-8eQqUgi4gyRbONIA130_assertion evidence source_evidence_literature NP1259648.RAGnB1NZ10kxCkiNeKuvnZQ_G8_O-8eQqUgi4gyRbONIA130_provenance.
- NP1259648.RAGnB1NZ10kxCkiNeKuvnZQ_G8_O-8eQqUgi4gyRbONIA130_assertion SIO_000772 25636564 NP1259648.RAGnB1NZ10kxCkiNeKuvnZQ_G8_O-8eQqUgi4gyRbONIA130_provenance.
- NP1259648.RAGnB1NZ10kxCkiNeKuvnZQ_G8_O-8eQqUgi4gyRbONIA130_assertion wasDerivedFrom befree-2016 NP1259648.RAGnB1NZ10kxCkiNeKuvnZQ_G8_O-8eQqUgi4gyRbONIA130_provenance.
- NP1259648.RAGnB1NZ10kxCkiNeKuvnZQ_G8_O-8eQqUgi4gyRbONIA130_assertion wasGeneratedBy ECO_0000203 NP1259648.RAGnB1NZ10kxCkiNeKuvnZQ_G8_O-8eQqUgi4gyRbONIA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1259648.RAGnB1NZ10kxCkiNeKuvnZQ_G8_O-8eQqUgi4gyRbONIA130_provenance.