Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP278517.RARmH9C9One0ZMGV1I2jA94RRLTU2OL8yeOastigVnXI4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP278517.RARmH9C9One0ZMGV1I2jA94RRLTU2OL8yeOastigVnXI4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP278517.RARmH9C9One0ZMGV1I2jA94RRLTU2OL8yeOastigVnXI4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP278517.RARmH9C9One0ZMGV1I2jA94RRLTU2OL8yeOastigVnXI4130_provenance.
- NP278517.RARmH9C9One0ZMGV1I2jA94RRLTU2OL8yeOastigVnXI4130_assertion description "[We report a rare case of double heterozygous type I protein C deficiency and factor V Leiden in a patient with classic myotonic dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP278517.RARmH9C9One0ZMGV1I2jA94RRLTU2OL8yeOastigVnXI4130_provenance.
- NP278517.RARmH9C9One0ZMGV1I2jA94RRLTU2OL8yeOastigVnXI4130_assertion evidence source_evidence_literature NP278517.RARmH9C9One0ZMGV1I2jA94RRLTU2OL8yeOastigVnXI4130_provenance.
- NP278517.RARmH9C9One0ZMGV1I2jA94RRLTU2OL8yeOastigVnXI4130_assertion SIO_000772 10726006 NP278517.RARmH9C9One0ZMGV1I2jA94RRLTU2OL8yeOastigVnXI4130_provenance.
- NP278517.RARmH9C9One0ZMGV1I2jA94RRLTU2OL8yeOastigVnXI4130_assertion wasDerivedFrom befree-2016 NP278517.RARmH9C9One0ZMGV1I2jA94RRLTU2OL8yeOastigVnXI4130_provenance.
- NP278517.RARmH9C9One0ZMGV1I2jA94RRLTU2OL8yeOastigVnXI4130_assertion wasGeneratedBy ECO_0000203 NP278517.RARmH9C9One0ZMGV1I2jA94RRLTU2OL8yeOastigVnXI4130_provenance.
- befree-2016 importedOn "2016-02-19" NP278517.RARmH9C9One0ZMGV1I2jA94RRLTU2OL8yeOastigVnXI4130_provenance.