Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP173584.RAf1fK4OEt8Lue7gk9yzPdPK6lw6FP1JiRIDzqAdwx92w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP173584.RAf1fK4OEt8Lue7gk9yzPdPK6lw6FP1JiRIDzqAdwx92w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP173584.RAf1fK4OEt8Lue7gk9yzPdPK6lw6FP1JiRIDzqAdwx92w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP173584.RAf1fK4OEt8Lue7gk9yzPdPK6lw6FP1JiRIDzqAdwx92w130_provenance.
- NP173584.RAf1fK4OEt8Lue7gk9yzPdPK6lw6FP1JiRIDzqAdwx92w130_assertion description "[We have analysed 142 unrelated patients and identified 141 factor VIII mutations and one Normandy type von Willebrand homozygote.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173584.RAf1fK4OEt8Lue7gk9yzPdPK6lw6FP1JiRIDzqAdwx92w130_provenance.
- NP173584.RAf1fK4OEt8Lue7gk9yzPdPK6lw6FP1JiRIDzqAdwx92w130_assertion evidence source_evidence_literature NP173584.RAf1fK4OEt8Lue7gk9yzPdPK6lw6FP1JiRIDzqAdwx92w130_provenance.
- NP173584.RAf1fK4OEt8Lue7gk9yzPdPK6lw6FP1JiRIDzqAdwx92w130_assertion SIO_000772 10404764 NP173584.RAf1fK4OEt8Lue7gk9yzPdPK6lw6FP1JiRIDzqAdwx92w130_provenance.
- NP173584.RAf1fK4OEt8Lue7gk9yzPdPK6lw6FP1JiRIDzqAdwx92w130_assertion wasDerivedFrom befree-20140225 NP173584.RAf1fK4OEt8Lue7gk9yzPdPK6lw6FP1JiRIDzqAdwx92w130_provenance.
- NP173584.RAf1fK4OEt8Lue7gk9yzPdPK6lw6FP1JiRIDzqAdwx92w130_assertion wasGeneratedBy ECO_0000203 NP173584.RAf1fK4OEt8Lue7gk9yzPdPK6lw6FP1JiRIDzqAdwx92w130_provenance.
- befree-20140225 importedOn "2014-02-25" NP173584.RAf1fK4OEt8Lue7gk9yzPdPK6lw6FP1JiRIDzqAdwx92w130_provenance.