Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP148302.RAzs35pzVK2ID4I3o2vpz1BuvFQJbhjfXPC35sdbI1tfk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP148302.RAzs35pzVK2ID4I3o2vpz1BuvFQJbhjfXPC35sdbI1tfk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP148302.RAzs35pzVK2ID4I3o2vpz1BuvFQJbhjfXPC35sdbI1tfk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP148302.RAzs35pzVK2ID4I3o2vpz1BuvFQJbhjfXPC35sdbI1tfk130_provenance.
- NP148302.RAzs35pzVK2ID4I3o2vpz1BuvFQJbhjfXPC35sdbI1tfk130_assertion description "[To provide a complete database of mutations and polymorphisms associated with factor XI deficiency, all available data on hereditary factor XI deficiency from main biological and medical databases were collected ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148302.RAzs35pzVK2ID4I3o2vpz1BuvFQJbhjfXPC35sdbI1tfk130_provenance.
- NP148302.RAzs35pzVK2ID4I3o2vpz1BuvFQJbhjfXPC35sdbI1tfk130_assertion evidence source_evidence_literature NP148302.RAzs35pzVK2ID4I3o2vpz1BuvFQJbhjfXPC35sdbI1tfk130_provenance.
- NP148302.RAzs35pzVK2ID4I3o2vpz1BuvFQJbhjfXPC35sdbI1tfk130_assertion SIO_000772 15870541 NP148302.RAzs35pzVK2ID4I3o2vpz1BuvFQJbhjfXPC35sdbI1tfk130_provenance.
- NP148302.RAzs35pzVK2ID4I3o2vpz1BuvFQJbhjfXPC35sdbI1tfk130_assertion wasDerivedFrom lhgdn-20090331 NP148302.RAzs35pzVK2ID4I3o2vpz1BuvFQJbhjfXPC35sdbI1tfk130_provenance.
- NP148302.RAzs35pzVK2ID4I3o2vpz1BuvFQJbhjfXPC35sdbI1tfk130_assertion wasGeneratedBy ECO_0000203 NP148302.RAzs35pzVK2ID4I3o2vpz1BuvFQJbhjfXPC35sdbI1tfk130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP148302.RAzs35pzVK2ID4I3o2vpz1BuvFQJbhjfXPC35sdbI1tfk130_provenance.