Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP7709.RA61cFT8-rfRo5pslywkvfsBm6aIyYXSlbsQ-Jr2zgWgw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP7709.RA61cFT8-rfRo5pslywkvfsBm6aIyYXSlbsQ-Jr2zgWgw130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP7709.RA61cFT8-rfRo5pslywkvfsBm6aIyYXSlbsQ-Jr2zgWgw130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP7709.RA61cFT8-rfRo5pslywkvfsBm6aIyYXSlbsQ-Jr2zgWgw130_provenance.
- NP7709.RA61cFT8-rfRo5pslywkvfsBm6aIyYXSlbsQ-Jr2zgWgw130_assertion description "[WDR34 mutations that cause short-rib polydactyly syndrome type III/severe asphyxiating thoracic dysplasia reveal a role for the NF-?B pathway in cilia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7709.RA61cFT8-rfRo5pslywkvfsBm6aIyYXSlbsQ-Jr2zgWgw130_provenance.
- NP7709.RA61cFT8-rfRo5pslywkvfsBm6aIyYXSlbsQ-Jr2zgWgw130_assertion evidence source_evidence_curated NP7709.RA61cFT8-rfRo5pslywkvfsBm6aIyYXSlbsQ-Jr2zgWgw130_provenance.
- NP7709.RA61cFT8-rfRo5pslywkvfsBm6aIyYXSlbsQ-Jr2zgWgw130_assertion SIO_000772 24183449 NP7709.RA61cFT8-rfRo5pslywkvfsBm6aIyYXSlbsQ-Jr2zgWgw130_provenance.
- NP7709.RA61cFT8-rfRo5pslywkvfsBm6aIyYXSlbsQ-Jr2zgWgw130_assertion wasDerivedFrom uniprot-2016 NP7709.RA61cFT8-rfRo5pslywkvfsBm6aIyYXSlbsQ-Jr2zgWgw130_provenance.
- NP7709.RA61cFT8-rfRo5pslywkvfsBm6aIyYXSlbsQ-Jr2zgWgw130_assertion wasGeneratedBy ECO_0000218 NP7709.RA61cFT8-rfRo5pslywkvfsBm6aIyYXSlbsQ-Jr2zgWgw130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP7709.RA61cFT8-rfRo5pslywkvfsBm6aIyYXSlbsQ-Jr2zgWgw130_provenance.