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- NP663768.RAZJJgWn-R-9YWs1MJzM0QoWoRI63NrRJ1iwGlkHY5rZg130_assertion type Assertion NP663768.RAZJJgWn-R-9YWs1MJzM0QoWoRI63NrRJ1iwGlkHY5rZg130_head.
- NP663768.RAZJJgWn-R-9YWs1MJzM0QoWoRI63NrRJ1iwGlkHY5rZg130_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." NP663768.RAZJJgWn-R-9YWs1MJzM0QoWoRI63NrRJ1iwGlkHY5rZg130_provenance.
- NP663768.RAZJJgWn-R-9YWs1MJzM0QoWoRI63NrRJ1iwGlkHY5rZg130_assertion evidence source_evidence_literature NP663768.RAZJJgWn-R-9YWs1MJzM0QoWoRI63NrRJ1iwGlkHY5rZg130_provenance.
- NP663768.RAZJJgWn-R-9YWs1MJzM0QoWoRI63NrRJ1iwGlkHY5rZg130_assertion SIO_000772 21314004 NP663768.RAZJJgWn-R-9YWs1MJzM0QoWoRI63NrRJ1iwGlkHY5rZg130_provenance.
- NP663768.RAZJJgWn-R-9YWs1MJzM0QoWoRI63NrRJ1iwGlkHY5rZg130_assertion wasDerivedFrom befree-20140225 NP663768.RAZJJgWn-R-9YWs1MJzM0QoWoRI63NrRJ1iwGlkHY5rZg130_provenance.
- NP663768.RAZJJgWn-R-9YWs1MJzM0QoWoRI63NrRJ1iwGlkHY5rZg130_assertion wasGeneratedBy ECO_0000203 NP663768.RAZJJgWn-R-9YWs1MJzM0QoWoRI63NrRJ1iwGlkHY5rZg130_provenance.