Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP5412.RAvqIOr9WrYDpZMp5kmnnsy42z5BfSyBF8Mr2TFwhhTtk130_assertion> ?p ?o ?g. }
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- NP5412.RAvqIOr9WrYDpZMp5kmnnsy42z5BfSyBF8Mr2TFwhhTtk130_assertion type Assertion NP5412.RAvqIOr9WrYDpZMp5kmnnsy42z5BfSyBF8Mr2TFwhhTtk130_head.
- NP5412.RAvqIOr9WrYDpZMp5kmnnsy42z5BfSyBF8Mr2TFwhhTtk130_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." NP5412.RAvqIOr9WrYDpZMp5kmnnsy42z5BfSyBF8Mr2TFwhhTtk130_provenance.
- NP5412.RAvqIOr9WrYDpZMp5kmnnsy42z5BfSyBF8Mr2TFwhhTtk130_assertion evidence source_evidence_curated NP5412.RAvqIOr9WrYDpZMp5kmnnsy42z5BfSyBF8Mr2TFwhhTtk130_provenance.
- NP5412.RAvqIOr9WrYDpZMp5kmnnsy42z5BfSyBF8Mr2TFwhhTtk130_assertion SIO_000772 12531900 NP5412.RAvqIOr9WrYDpZMp5kmnnsy42z5BfSyBF8Mr2TFwhhTtk130_provenance.
- NP5412.RAvqIOr9WrYDpZMp5kmnnsy42z5BfSyBF8Mr2TFwhhTtk130_assertion wasDerivedFrom uniprot-20130724 NP5412.RAvqIOr9WrYDpZMp5kmnnsy42z5BfSyBF8Mr2TFwhhTtk130_provenance.
- NP5412.RAvqIOr9WrYDpZMp5kmnnsy42z5BfSyBF8Mr2TFwhhTtk130_assertion wasGeneratedBy ECO_0000218 NP5412.RAvqIOr9WrYDpZMp5kmnnsy42z5BfSyBF8Mr2TFwhhTtk130_provenance.