Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP17892.RAkr5-3N7qN-ZPb1soB50yp4Ulz0a-Ac4mDw6DRdQedb8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP17892.RAkr5-3N7qN-ZPb1soB50yp4Ulz0a-Ac4mDw6DRdQedb8130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP17892.RAkr5-3N7qN-ZPb1soB50yp4Ulz0a-Ac4mDw6DRdQedb8130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP17892.RAkr5-3N7qN-ZPb1soB50yp4Ulz0a-Ac4mDw6DRdQedb8130_provenance.
- NP17892.RAkr5-3N7qN-ZPb1soB50yp4Ulz0a-Ac4mDw6DRdQedb8130_assertion wasGeneratedBy ECO_0000218 NP17892.RAkr5-3N7qN-ZPb1soB50yp4Ulz0a-Ac4mDw6DRdQedb8130_provenance.
- NP17892.RAkr5-3N7qN-ZPb1soB50yp4Ulz0a-Ac4mDw6DRdQedb8130_assertion wasDerivedFrom ctd_human-20130708 NP17892.RAkr5-3N7qN-ZPb1soB50yp4Ulz0a-Ac4mDw6DRdQedb8130_provenance.
- NP17892.RAkr5-3N7qN-ZPb1soB50yp4Ulz0a-Ac4mDw6DRdQedb8130_assertion SIO_000772 22961002 NP17892.RAkr5-3N7qN-ZPb1soB50yp4Ulz0a-Ac4mDw6DRdQedb8130_provenance.
- NP17892.RAkr5-3N7qN-ZPb1soB50yp4Ulz0a-Ac4mDw6DRdQedb8130_assertion evidence source_evidence_curated NP17892.RAkr5-3N7qN-ZPb1soB50yp4Ulz0a-Ac4mDw6DRdQedb8130_provenance.
- NP17892.RAkr5-3N7qN-ZPb1soB50yp4Ulz0a-Ac4mDw6DRdQedb8130_assertion description "[Our study provides evidence that loss of functional HINT1 protein results in a distinct phenotype of autosomal recessive axonal neuropathy with neuromyotonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP17892.RAkr5-3N7qN-ZPb1soB50yp4Ulz0a-Ac4mDw6DRdQedb8130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP17892.RAkr5-3N7qN-ZPb1soB50yp4Ulz0a-Ac4mDw6DRdQedb8130_provenance.