Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP213766.RAJhObQOipiX8Nv9tip1N5NcgAXcSVFvu6r2SsbaEK4Ks130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP213766.RAJhObQOipiX8Nv9tip1N5NcgAXcSVFvu6r2SsbaEK4Ks130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP213766.RAJhObQOipiX8Nv9tip1N5NcgAXcSVFvu6r2SsbaEK4Ks130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP213766.RAJhObQOipiX8Nv9tip1N5NcgAXcSVFvu6r2SsbaEK4Ks130_provenance.
- NP213766.RAJhObQOipiX8Nv9tip1N5NcgAXcSVFvu6r2SsbaEK4Ks130_assertion description "[A novel RUNX2 missense mutation has been found in members of a family clinically diagnosed with cleidocranial dysplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP213766.RAJhObQOipiX8Nv9tip1N5NcgAXcSVFvu6r2SsbaEK4Ks130_provenance.
- NP213766.RAJhObQOipiX8Nv9tip1N5NcgAXcSVFvu6r2SsbaEK4Ks130_assertion evidence source_evidence_literature NP213766.RAJhObQOipiX8Nv9tip1N5NcgAXcSVFvu6r2SsbaEK4Ks130_provenance.
- NP213766.RAJhObQOipiX8Nv9tip1N5NcgAXcSVFvu6r2SsbaEK4Ks130_assertion SIO_000772 16244783 NP213766.RAJhObQOipiX8Nv9tip1N5NcgAXcSVFvu6r2SsbaEK4Ks130_provenance.
- NP213766.RAJhObQOipiX8Nv9tip1N5NcgAXcSVFvu6r2SsbaEK4Ks130_assertion wasDerivedFrom lhgdn-20090331 NP213766.RAJhObQOipiX8Nv9tip1N5NcgAXcSVFvu6r2SsbaEK4Ks130_provenance.
- NP213766.RAJhObQOipiX8Nv9tip1N5NcgAXcSVFvu6r2SsbaEK4Ks130_assertion wasGeneratedBy ECO_0000203 NP213766.RAJhObQOipiX8Nv9tip1N5NcgAXcSVFvu6r2SsbaEK4Ks130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP213766.RAJhObQOipiX8Nv9tip1N5NcgAXcSVFvu6r2SsbaEK4Ks130_provenance.