Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP203877.RAT1V88_2UxS_hwHoIhR1FPmItbRy8voeLhJo81zfoJvE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP203877.RAT1V88_2UxS_hwHoIhR1FPmItbRy8voeLhJo81zfoJvE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP203877.RAT1V88_2UxS_hwHoIhR1FPmItbRy8voeLhJo81zfoJvE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP203877.RAT1V88_2UxS_hwHoIhR1FPmItbRy8voeLhJo81zfoJvE130_provenance.
- NP203877.RAT1V88_2UxS_hwHoIhR1FPmItbRy8voeLhJo81zfoJvE130_assertion description "[These findings suggest that mutations in beta actin may be associated with a broad spectrum of developmental malformations and/or neurological abnormalities such as dystonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP203877.RAT1V88_2UxS_hwHoIhR1FPmItbRy8voeLhJo81zfoJvE130_provenance.
- NP203877.RAT1V88_2UxS_hwHoIhR1FPmItbRy8voeLhJo81zfoJvE130_assertion evidence source_evidence_literature NP203877.RAT1V88_2UxS_hwHoIhR1FPmItbRy8voeLhJo81zfoJvE130_provenance.
- NP203877.RAT1V88_2UxS_hwHoIhR1FPmItbRy8voeLhJo81zfoJvE130_assertion SIO_000772 16685646 NP203877.RAT1V88_2UxS_hwHoIhR1FPmItbRy8voeLhJo81zfoJvE130_provenance.
- NP203877.RAT1V88_2UxS_hwHoIhR1FPmItbRy8voeLhJo81zfoJvE130_assertion wasDerivedFrom lhgdn-20090331 NP203877.RAT1V88_2UxS_hwHoIhR1FPmItbRy8voeLhJo81zfoJvE130_provenance.
- NP203877.RAT1V88_2UxS_hwHoIhR1FPmItbRy8voeLhJo81zfoJvE130_assertion wasGeneratedBy ECO_0000203 NP203877.RAT1V88_2UxS_hwHoIhR1FPmItbRy8voeLhJo81zfoJvE130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP203877.RAT1V88_2UxS_hwHoIhR1FPmItbRy8voeLhJo81zfoJvE130_provenance.