Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP2813.RAY2olYbKE9gWVjrGnUGZc3dzlUhsd1YATMMd8OZoHB98130_assertion> ?p ?o ?g. }
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- NP2813.RAY2olYbKE9gWVjrGnUGZc3dzlUhsd1YATMMd8OZoHB98130_assertion type Assertion NP2813.RAY2olYbKE9gWVjrGnUGZc3dzlUhsd1YATMMd8OZoHB98130_head.
- NP2813.RAY2olYbKE9gWVjrGnUGZc3dzlUhsd1YATMMd8OZoHB98130_assertion description "[Characterization of the molecular defects in Rab27a, caused by RAB27A missense mutations found in patients with Griscelli syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2813.RAY2olYbKE9gWVjrGnUGZc3dzlUhsd1YATMMd8OZoHB98130_provenance.
- NP2813.RAY2olYbKE9gWVjrGnUGZc3dzlUhsd1YATMMd8OZoHB98130_assertion evidence source_evidence_curated NP2813.RAY2olYbKE9gWVjrGnUGZc3dzlUhsd1YATMMd8OZoHB98130_provenance.
- NP2813.RAY2olYbKE9gWVjrGnUGZc3dzlUhsd1YATMMd8OZoHB98130_assertion SIO_000772 12531900 NP2813.RAY2olYbKE9gWVjrGnUGZc3dzlUhsd1YATMMd8OZoHB98130_provenance.
- NP2813.RAY2olYbKE9gWVjrGnUGZc3dzlUhsd1YATMMd8OZoHB98130_assertion wasDerivedFrom uniprot-20150221 NP2813.RAY2olYbKE9gWVjrGnUGZc3dzlUhsd1YATMMd8OZoHB98130_provenance.
- NP2813.RAY2olYbKE9gWVjrGnUGZc3dzlUhsd1YATMMd8OZoHB98130_assertion wasGeneratedBy ECO_0000218 NP2813.RAY2olYbKE9gWVjrGnUGZc3dzlUhsd1YATMMd8OZoHB98130_provenance.