Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP924777.RA4ApdTttCUmCW33oATrLr2sJd5loF4TuOZe1FenwZ5UQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP924777.RA4ApdTttCUmCW33oATrLr2sJd5loF4TuOZe1FenwZ5UQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP924777.RA4ApdTttCUmCW33oATrLr2sJd5loF4TuOZe1FenwZ5UQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP924777.RA4ApdTttCUmCW33oATrLr2sJd5loF4TuOZe1FenwZ5UQ130_provenance.
- NP924777.RA4ApdTttCUmCW33oATrLr2sJd5loF4TuOZe1FenwZ5UQ130_assertion description "[We have shown previously that the ubiquitin ligase MID1, mutations of which cause the midline malformation Opitz BBB/G syndrome (OS), serves as scaffold for a microtubule-associated protein complex that regulates protein phosphatase 2A (PP2A) activity in a ubiquitin-dependent manner.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP924777.RA4ApdTttCUmCW33oATrLr2sJd5loF4TuOZe1FenwZ5UQ130_provenance.
- NP924777.RA4ApdTttCUmCW33oATrLr2sJd5loF4TuOZe1FenwZ5UQ130_assertion evidence source_evidence_literature NP924777.RA4ApdTttCUmCW33oATrLr2sJd5loF4TuOZe1FenwZ5UQ130_provenance.
- NP924777.RA4ApdTttCUmCW33oATrLr2sJd5loF4TuOZe1FenwZ5UQ130_assertion SIO_000772 21930711 NP924777.RA4ApdTttCUmCW33oATrLr2sJd5loF4TuOZe1FenwZ5UQ130_provenance.
- NP924777.RA4ApdTttCUmCW33oATrLr2sJd5loF4TuOZe1FenwZ5UQ130_assertion wasDerivedFrom befree-2016 NP924777.RA4ApdTttCUmCW33oATrLr2sJd5loF4TuOZe1FenwZ5UQ130_provenance.
- NP924777.RA4ApdTttCUmCW33oATrLr2sJd5loF4TuOZe1FenwZ5UQ130_assertion wasGeneratedBy ECO_0000203 NP924777.RA4ApdTttCUmCW33oATrLr2sJd5loF4TuOZe1FenwZ5UQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP924777.RA4ApdTttCUmCW33oATrLr2sJd5loF4TuOZe1FenwZ5UQ130_provenance.