Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP121388.RAbMIhF9Qu9xWFZsn_rFeKC9_zF1VeKzuwReyrZzFZp2U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP121388.RAbMIhF9Qu9xWFZsn_rFeKC9_zF1VeKzuwReyrZzFZp2U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP121388.RAbMIhF9Qu9xWFZsn_rFeKC9_zF1VeKzuwReyrZzFZp2U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP121388.RAbMIhF9Qu9xWFZsn_rFeKC9_zF1VeKzuwReyrZzFZp2U130_provenance.
- NP121388.RAbMIhF9Qu9xWFZsn_rFeKC9_zF1VeKzuwReyrZzFZp2U130_assertion description "[Common genetic variants in candidate genes and risk of familial lymphoid malignancies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP121388.RAbMIhF9Qu9xWFZsn_rFeKC9_zF1VeKzuwReyrZzFZp2U130_provenance.
- NP121388.RAbMIhF9Qu9xWFZsn_rFeKC9_zF1VeKzuwReyrZzFZp2U130_assertion evidence source_evidence_literature NP121388.RAbMIhF9Qu9xWFZsn_rFeKC9_zF1VeKzuwReyrZzFZp2U130_provenance.
- NP121388.RAbMIhF9Qu9xWFZsn_rFeKC9_zF1VeKzuwReyrZzFZp2U130_assertion SIO_000772 19573080 NP121388.RAbMIhF9Qu9xWFZsn_rFeKC9_zF1VeKzuwReyrZzFZp2U130_provenance.
- NP121388.RAbMIhF9Qu9xWFZsn_rFeKC9_zF1VeKzuwReyrZzFZp2U130_assertion wasDerivedFrom gad-20150221 NP121388.RAbMIhF9Qu9xWFZsn_rFeKC9_zF1VeKzuwReyrZzFZp2U130_provenance.
- NP121388.RAbMIhF9Qu9xWFZsn_rFeKC9_zF1VeKzuwReyrZzFZp2U130_assertion wasGeneratedBy ECO_0000203 NP121388.RAbMIhF9Qu9xWFZsn_rFeKC9_zF1VeKzuwReyrZzFZp2U130_provenance.
- gad-20150221 importedOn "2015-02-21" NP121388.RAbMIhF9Qu9xWFZsn_rFeKC9_zF1VeKzuwReyrZzFZp2U130_provenance.