Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP3493.RAH0bTker4E4AEdQguvOmUNjYVqvAVG-tBFrC_2urA7i0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP3493.RAH0bTker4E4AEdQguvOmUNjYVqvAVG-tBFrC_2urA7i0130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP3493.RAH0bTker4E4AEdQguvOmUNjYVqvAVG-tBFrC_2urA7i0130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP3493.RAH0bTker4E4AEdQguvOmUNjYVqvAVG-tBFrC_2urA7i0130_provenance.
- NP3493.RAH0bTker4E4AEdQguvOmUNjYVqvAVG-tBFrC_2urA7i0130_assertion description "[Evidence for a dominant-negative effect in ACTA1 nemaline myopathy caused by abnormal folding, aggregation and altered polymerization of mutant actin isoforms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3493.RAH0bTker4E4AEdQguvOmUNjYVqvAVG-tBFrC_2urA7i0130_provenance.
- NP3493.RAH0bTker4E4AEdQguvOmUNjYVqvAVG-tBFrC_2urA7i0130_assertion evidence source_evidence_curated NP3493.RAH0bTker4E4AEdQguvOmUNjYVqvAVG-tBFrC_2urA7i0130_provenance.
- NP3493.RAH0bTker4E4AEdQguvOmUNjYVqvAVG-tBFrC_2urA7i0130_assertion SIO_000772 15198992 NP3493.RAH0bTker4E4AEdQguvOmUNjYVqvAVG-tBFrC_2urA7i0130_provenance.
- NP3493.RAH0bTker4E4AEdQguvOmUNjYVqvAVG-tBFrC_2urA7i0130_assertion wasDerivedFrom uniprot-2016 NP3493.RAH0bTker4E4AEdQguvOmUNjYVqvAVG-tBFrC_2urA7i0130_provenance.
- NP3493.RAH0bTker4E4AEdQguvOmUNjYVqvAVG-tBFrC_2urA7i0130_assertion wasGeneratedBy ECO_0000218 NP3493.RAH0bTker4E4AEdQguvOmUNjYVqvAVG-tBFrC_2urA7i0130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP3493.RAH0bTker4E4AEdQguvOmUNjYVqvAVG-tBFrC_2urA7i0130_provenance.