Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP662850.RAiPr5U3K5QaEcDvQXqgjRHPJE6hEx2rtuTQ9U7jI_6Ts130_assertion> ?p ?o ?g. }
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- NP662850.RAiPr5U3K5QaEcDvQXqgjRHPJE6hEx2rtuTQ9U7jI_6Ts130_assertion type Assertion NP662850.RAiPr5U3K5QaEcDvQXqgjRHPJE6hEx2rtuTQ9U7jI_6Ts130_head.
- NP662850.RAiPr5U3K5QaEcDvQXqgjRHPJE6hEx2rtuTQ9U7jI_6Ts130_assertion description "[Griscelli syndrome type 2 is a rare autosomal recessive primary immunodeficiency disease caused by a mutation in the RAB27A gene and characterized by oculocutaneous hypopigmentation and variable cellular immunodeficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP662850.RAiPr5U3K5QaEcDvQXqgjRHPJE6hEx2rtuTQ9U7jI_6Ts130_provenance.
- NP662850.RAiPr5U3K5QaEcDvQXqgjRHPJE6hEx2rtuTQ9U7jI_6Ts130_assertion evidence source_evidence_literature NP662850.RAiPr5U3K5QaEcDvQXqgjRHPJE6hEx2rtuTQ9U7jI_6Ts130_provenance.
- NP662850.RAiPr5U3K5QaEcDvQXqgjRHPJE6hEx2rtuTQ9U7jI_6Ts130_assertion SIO_000772 21314004 NP662850.RAiPr5U3K5QaEcDvQXqgjRHPJE6hEx2rtuTQ9U7jI_6Ts130_provenance.
- NP662850.RAiPr5U3K5QaEcDvQXqgjRHPJE6hEx2rtuTQ9U7jI_6Ts130_assertion wasDerivedFrom befree-20150227 NP662850.RAiPr5U3K5QaEcDvQXqgjRHPJE6hEx2rtuTQ9U7jI_6Ts130_provenance.
- NP662850.RAiPr5U3K5QaEcDvQXqgjRHPJE6hEx2rtuTQ9U7jI_6Ts130_assertion wasGeneratedBy ECO_0000203 NP662850.RAiPr5U3K5QaEcDvQXqgjRHPJE6hEx2rtuTQ9U7jI_6Ts130_provenance.