Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1261057.RAO93fP87GP1pNxzitiuFKevLKEcfVYjYsRcKUG3f7FVc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1261057.RAO93fP87GP1pNxzitiuFKevLKEcfVYjYsRcKUG3f7FVc130_assertion type Assertion NP1261057.RAO93fP87GP1pNxzitiuFKevLKEcfVYjYsRcKUG3f7FVc130_head.
- NP1261057.RAO93fP87GP1pNxzitiuFKevLKEcfVYjYsRcKUG3f7FVc130_assertion description "[TTC19 mutations constitute a rare cause of CIII deficiency and are associated with neurological disorders in childhood and adulthood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1261057.RAO93fP87GP1pNxzitiuFKevLKEcfVYjYsRcKUG3f7FVc130_provenance.
- NP1261057.RAO93fP87GP1pNxzitiuFKevLKEcfVYjYsRcKUG3f7FVc130_assertion evidence source_evidence_literature NP1261057.RAO93fP87GP1pNxzitiuFKevLKEcfVYjYsRcKUG3f7FVc130_provenance.
- NP1261057.RAO93fP87GP1pNxzitiuFKevLKEcfVYjYsRcKUG3f7FVc130_assertion SIO_000772 25652355 NP1261057.RAO93fP87GP1pNxzitiuFKevLKEcfVYjYsRcKUG3f7FVc130_provenance.
- NP1261057.RAO93fP87GP1pNxzitiuFKevLKEcfVYjYsRcKUG3f7FVc130_assertion wasDerivedFrom befree-2016 NP1261057.RAO93fP87GP1pNxzitiuFKevLKEcfVYjYsRcKUG3f7FVc130_provenance.
- NP1261057.RAO93fP87GP1pNxzitiuFKevLKEcfVYjYsRcKUG3f7FVc130_assertion wasGeneratedBy ECO_0000203 NP1261057.RAO93fP87GP1pNxzitiuFKevLKEcfVYjYsRcKUG3f7FVc130_provenance.