Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP212454.RASud7UjBM6ZEFkUE8BBxY7o_FMhogkhsLvtAVuFZx0Vo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP212454.RASud7UjBM6ZEFkUE8BBxY7o_FMhogkhsLvtAVuFZx0Vo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP212454.RASud7UjBM6ZEFkUE8BBxY7o_FMhogkhsLvtAVuFZx0Vo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP212454.RASud7UjBM6ZEFkUE8BBxY7o_FMhogkhsLvtAVuFZx0Vo130_provenance.
- NP212454.RASud7UjBM6ZEFkUE8BBxY7o_FMhogkhsLvtAVuFZx0Vo130_assertion description "[Here we report that mice lacking the transmembrane protein Cdo, previously implicated in myogenesis, display HPE with strain-specific severity and without limb defects, modeling human HPE and implicating modifier genes as a cause of variability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP212454.RASud7UjBM6ZEFkUE8BBxY7o_FMhogkhsLvtAVuFZx0Vo130_provenance.
- NP212454.RASud7UjBM6ZEFkUE8BBxY7o_FMhogkhsLvtAVuFZx0Vo130_assertion evidence source_evidence_literature NP212454.RASud7UjBM6ZEFkUE8BBxY7o_FMhogkhsLvtAVuFZx0Vo130_provenance.
- NP212454.RASud7UjBM6ZEFkUE8BBxY7o_FMhogkhsLvtAVuFZx0Vo130_assertion SIO_000772 16647303 NP212454.RASud7UjBM6ZEFkUE8BBxY7o_FMhogkhsLvtAVuFZx0Vo130_provenance.
- NP212454.RASud7UjBM6ZEFkUE8BBxY7o_FMhogkhsLvtAVuFZx0Vo130_assertion wasDerivedFrom befree-20140225 NP212454.RASud7UjBM6ZEFkUE8BBxY7o_FMhogkhsLvtAVuFZx0Vo130_provenance.
- NP212454.RASud7UjBM6ZEFkUE8BBxY7o_FMhogkhsLvtAVuFZx0Vo130_assertion wasGeneratedBy ECO_0000203 NP212454.RASud7UjBM6ZEFkUE8BBxY7o_FMhogkhsLvtAVuFZx0Vo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP212454.RASud7UjBM6ZEFkUE8BBxY7o_FMhogkhsLvtAVuFZx0Vo130_provenance.