Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP924788.RA2lGbx18LouwoG8Vl5nz4nI5LWI-rbk437tJHbjun0Lw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP924788.RA2lGbx18LouwoG8Vl5nz4nI5LWI-rbk437tJHbjun0Lw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP924788.RA2lGbx18LouwoG8Vl5nz4nI5LWI-rbk437tJHbjun0Lw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP924788.RA2lGbx18LouwoG8Vl5nz4nI5LWI-rbk437tJHbjun0Lw130_provenance.
- NP924788.RA2lGbx18LouwoG8Vl5nz4nI5LWI-rbk437tJHbjun0Lw130_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." NP924788.RA2lGbx18LouwoG8Vl5nz4nI5LWI-rbk437tJHbjun0Lw130_provenance.
- NP924788.RA2lGbx18LouwoG8Vl5nz4nI5LWI-rbk437tJHbjun0Lw130_assertion evidence source_evidence_literature NP924788.RA2lGbx18LouwoG8Vl5nz4nI5LWI-rbk437tJHbjun0Lw130_provenance.
- NP924788.RA2lGbx18LouwoG8Vl5nz4nI5LWI-rbk437tJHbjun0Lw130_assertion SIO_000772 21930711 NP924788.RA2lGbx18LouwoG8Vl5nz4nI5LWI-rbk437tJHbjun0Lw130_provenance.
- NP924788.RA2lGbx18LouwoG8Vl5nz4nI5LWI-rbk437tJHbjun0Lw130_assertion wasDerivedFrom befree-2016 NP924788.RA2lGbx18LouwoG8Vl5nz4nI5LWI-rbk437tJHbjun0Lw130_provenance.
- NP924788.RA2lGbx18LouwoG8Vl5nz4nI5LWI-rbk437tJHbjun0Lw130_assertion wasGeneratedBy ECO_0000203 NP924788.RA2lGbx18LouwoG8Vl5nz4nI5LWI-rbk437tJHbjun0Lw130_provenance.
- befree-2016 importedOn "2016-02-19" NP924788.RA2lGbx18LouwoG8Vl5nz4nI5LWI-rbk437tJHbjun0Lw130_provenance.