Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP260913.RAbPYomtkDvkD4bkk-P5kZ7OpwKIVlRsfA56UBQSxWZd0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP260913.RAbPYomtkDvkD4bkk-P5kZ7OpwKIVlRsfA56UBQSxWZd0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP260913.RAbPYomtkDvkD4bkk-P5kZ7OpwKIVlRsfA56UBQSxWZd0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP260913.RAbPYomtkDvkD4bkk-P5kZ7OpwKIVlRsfA56UBQSxWZd0130_provenance.
- NP260913.RAbPYomtkDvkD4bkk-P5kZ7OpwKIVlRsfA56UBQSxWZd0130_assertion description "[The proportion of NPC cases attributable to the GG CCND1 genotype was 14.76%.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP260913.RAbPYomtkDvkD4bkk-P5kZ7OpwKIVlRsfA56UBQSxWZd0130_provenance.
- NP260913.RAbPYomtkDvkD4bkk-P5kZ7OpwKIVlRsfA56UBQSxWZd0130_assertion evidence source_evidence_literature NP260913.RAbPYomtkDvkD4bkk-P5kZ7OpwKIVlRsfA56UBQSxWZd0130_provenance.
- NP260913.RAbPYomtkDvkD4bkk-P5kZ7OpwKIVlRsfA56UBQSxWZd0130_assertion SIO_000772 16691558 NP260913.RAbPYomtkDvkD4bkk-P5kZ7OpwKIVlRsfA56UBQSxWZd0130_provenance.
- NP260913.RAbPYomtkDvkD4bkk-P5kZ7OpwKIVlRsfA56UBQSxWZd0130_assertion wasDerivedFrom befree-20150227 NP260913.RAbPYomtkDvkD4bkk-P5kZ7OpwKIVlRsfA56UBQSxWZd0130_provenance.
- NP260913.RAbPYomtkDvkD4bkk-P5kZ7OpwKIVlRsfA56UBQSxWZd0130_assertion wasGeneratedBy ECO_0000203 NP260913.RAbPYomtkDvkD4bkk-P5kZ7OpwKIVlRsfA56UBQSxWZd0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP260913.RAbPYomtkDvkD4bkk-P5kZ7OpwKIVlRsfA56UBQSxWZd0130_provenance.