Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP215060.RAqUgaRKj9Zh88vI5bRDYPhieUBhUa0WjB4pppif0Z7GM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP215060.RAqUgaRKj9Zh88vI5bRDYPhieUBhUa0WjB4pppif0Z7GM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP215060.RAqUgaRKj9Zh88vI5bRDYPhieUBhUa0WjB4pppif0Z7GM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP215060.RAqUgaRKj9Zh88vI5bRDYPhieUBhUa0WjB4pppif0Z7GM130_provenance.
- NP215060.RAqUgaRKj9Zh88vI5bRDYPhieUBhUa0WjB4pppif0Z7GM130_assertion description "[novel nonsense mutations in 2 African American siblings with autosomal recessive Alport syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP215060.RAqUgaRKj9Zh88vI5bRDYPhieUBhUa0WjB4pppif0Z7GM130_provenance.
- NP215060.RAqUgaRKj9Zh88vI5bRDYPhieUBhUa0WjB4pppif0Z7GM130_assertion evidence source_evidence_literature NP215060.RAqUgaRKj9Zh88vI5bRDYPhieUBhUa0WjB4pppif0Z7GM130_provenance.
- NP215060.RAqUgaRKj9Zh88vI5bRDYPhieUBhUa0WjB4pppif0Z7GM130_assertion SIO_000772 18436078 NP215060.RAqUgaRKj9Zh88vI5bRDYPhieUBhUa0WjB4pppif0Z7GM130_provenance.
- NP215060.RAqUgaRKj9Zh88vI5bRDYPhieUBhUa0WjB4pppif0Z7GM130_assertion wasDerivedFrom lhgdn-20090331 NP215060.RAqUgaRKj9Zh88vI5bRDYPhieUBhUa0WjB4pppif0Z7GM130_provenance.
- NP215060.RAqUgaRKj9Zh88vI5bRDYPhieUBhUa0WjB4pppif0Z7GM130_assertion wasGeneratedBy ECO_0000203 NP215060.RAqUgaRKj9Zh88vI5bRDYPhieUBhUa0WjB4pppif0Z7GM130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP215060.RAqUgaRKj9Zh88vI5bRDYPhieUBhUa0WjB4pppif0Z7GM130_provenance.