Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP599824.RACzpsBWSOmrFD2x6dbVxXx895YFidyh-wgwrWu7hksEw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP599824.RACzpsBWSOmrFD2x6dbVxXx895YFidyh-wgwrWu7hksEw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP599824.RACzpsBWSOmrFD2x6dbVxXx895YFidyh-wgwrWu7hksEw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP599824.RACzpsBWSOmrFD2x6dbVxXx895YFidyh-wgwrWu7hksEw130_provenance.
- NP599824.RACzpsBWSOmrFD2x6dbVxXx895YFidyh-wgwrWu7hksEw130_assertion description "[Today, more than 60 mutations in the factor XIIIA- and B-subunit genes are known leading to congenital factor XIII deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP599824.RACzpsBWSOmrFD2x6dbVxXx895YFidyh-wgwrWu7hksEw130_provenance.
- NP599824.RACzpsBWSOmrFD2x6dbVxXx895YFidyh-wgwrWu7hksEw130_assertion evidence source_evidence_literature NP599824.RACzpsBWSOmrFD2x6dbVxXx895YFidyh-wgwrWu7hksEw130_provenance.
- NP599824.RACzpsBWSOmrFD2x6dbVxXx895YFidyh-wgwrWu7hksEw130_assertion SIO_000772 16543965 NP599824.RACzpsBWSOmrFD2x6dbVxXx895YFidyh-wgwrWu7hksEw130_provenance.
- NP599824.RACzpsBWSOmrFD2x6dbVxXx895YFidyh-wgwrWu7hksEw130_assertion wasDerivedFrom befree-20140225 NP599824.RACzpsBWSOmrFD2x6dbVxXx895YFidyh-wgwrWu7hksEw130_provenance.
- NP599824.RACzpsBWSOmrFD2x6dbVxXx895YFidyh-wgwrWu7hksEw130_assertion wasGeneratedBy ECO_0000203 NP599824.RACzpsBWSOmrFD2x6dbVxXx895YFidyh-wgwrWu7hksEw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP599824.RACzpsBWSOmrFD2x6dbVxXx895YFidyh-wgwrWu7hksEw130_provenance.