Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP210959.RAbhvsaivlaWKXoKxUtoCr7objimhwcZBfX74A7GB4bCk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP210959.RAbhvsaivlaWKXoKxUtoCr7objimhwcZBfX74A7GB4bCk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP210959.RAbhvsaivlaWKXoKxUtoCr7objimhwcZBfX74A7GB4bCk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP210959.RAbhvsaivlaWKXoKxUtoCr7objimhwcZBfX74A7GB4bCk130_provenance.
- NP210959.RAbhvsaivlaWKXoKxUtoCr7objimhwcZBfX74A7GB4bCk130_assertion description "[Missense mutations c.341A > T (p.Asp113Val) in exon 4 and c.663T > G (p.Asn220Lys) in exon 7 are associated with hereditary nonspherocytic hemolytic anemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP210959.RAbhvsaivlaWKXoKxUtoCr7objimhwcZBfX74A7GB4bCk130_provenance.
- NP210959.RAbhvsaivlaWKXoKxUtoCr7objimhwcZBfX74A7GB4bCk130_assertion evidence source_evidence_literature NP210959.RAbhvsaivlaWKXoKxUtoCr7objimhwcZBfX74A7GB4bCk130_provenance.
- NP210959.RAbhvsaivlaWKXoKxUtoCr7objimhwcZBfX74A7GB4bCk130_assertion SIO_000772 17041899 NP210959.RAbhvsaivlaWKXoKxUtoCr7objimhwcZBfX74A7GB4bCk130_provenance.
- NP210959.RAbhvsaivlaWKXoKxUtoCr7objimhwcZBfX74A7GB4bCk130_assertion wasDerivedFrom lhgdn-20090331 NP210959.RAbhvsaivlaWKXoKxUtoCr7objimhwcZBfX74A7GB4bCk130_provenance.
- NP210959.RAbhvsaivlaWKXoKxUtoCr7objimhwcZBfX74A7GB4bCk130_assertion wasGeneratedBy ECO_0000203 NP210959.RAbhvsaivlaWKXoKxUtoCr7objimhwcZBfX74A7GB4bCk130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP210959.RAbhvsaivlaWKXoKxUtoCr7objimhwcZBfX74A7GB4bCk130_provenance.