Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP287484.RAwlhNGIaVTOKumnPM8bLu9ctWeGLXM-dY97HvRK9_Uqo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP287484.RAwlhNGIaVTOKumnPM8bLu9ctWeGLXM-dY97HvRK9_Uqo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP287484.RAwlhNGIaVTOKumnPM8bLu9ctWeGLXM-dY97HvRK9_Uqo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP287484.RAwlhNGIaVTOKumnPM8bLu9ctWeGLXM-dY97HvRK9_Uqo130_provenance.
- NP287484.RAwlhNGIaVTOKumnPM8bLu9ctWeGLXM-dY97HvRK9_Uqo130_assertion description "[Loss of p53 sensitizes mice with a mutation in Ccm1 (KRIT1) to development of cerebral vascular malformations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP287484.RAwlhNGIaVTOKumnPM8bLu9ctWeGLXM-dY97HvRK9_Uqo130_provenance.
- NP287484.RAwlhNGIaVTOKumnPM8bLu9ctWeGLXM-dY97HvRK9_Uqo130_assertion evidence source_evidence_literature NP287484.RAwlhNGIaVTOKumnPM8bLu9ctWeGLXM-dY97HvRK9_Uqo130_provenance.
- NP287484.RAwlhNGIaVTOKumnPM8bLu9ctWeGLXM-dY97HvRK9_Uqo130_assertion SIO_000772 15509522 NP287484.RAwlhNGIaVTOKumnPM8bLu9ctWeGLXM-dY97HvRK9_Uqo130_provenance.
- NP287484.RAwlhNGIaVTOKumnPM8bLu9ctWeGLXM-dY97HvRK9_Uqo130_assertion wasDerivedFrom befree-20150227 NP287484.RAwlhNGIaVTOKumnPM8bLu9ctWeGLXM-dY97HvRK9_Uqo130_provenance.
- NP287484.RAwlhNGIaVTOKumnPM8bLu9ctWeGLXM-dY97HvRK9_Uqo130_assertion wasGeneratedBy ECO_0000203 NP287484.RAwlhNGIaVTOKumnPM8bLu9ctWeGLXM-dY97HvRK9_Uqo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP287484.RAwlhNGIaVTOKumnPM8bLu9ctWeGLXM-dY97HvRK9_Uqo130_provenance.