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- NP871755.RAlXW5vR_N0Wc5A-nb2oz8IS3hpGBSzqBQf1-iN9BWSwU130_assertion type Assertion NP871755.RAlXW5vR_N0Wc5A-nb2oz8IS3hpGBSzqBQf1-iN9BWSwU130_head.
- NP871755.RAlXW5vR_N0Wc5A-nb2oz8IS3hpGBSzqBQf1-iN9BWSwU130_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." NP871755.RAlXW5vR_N0Wc5A-nb2oz8IS3hpGBSzqBQf1-iN9BWSwU130_provenance.
- NP871755.RAlXW5vR_N0Wc5A-nb2oz8IS3hpGBSzqBQf1-iN9BWSwU130_assertion evidence source_evidence_literature NP871755.RAlXW5vR_N0Wc5A-nb2oz8IS3hpGBSzqBQf1-iN9BWSwU130_provenance.
- NP871755.RAlXW5vR_N0Wc5A-nb2oz8IS3hpGBSzqBQf1-iN9BWSwU130_assertion SIO_000772 21314004 NP871755.RAlXW5vR_N0Wc5A-nb2oz8IS3hpGBSzqBQf1-iN9BWSwU130_provenance.
- NP871755.RAlXW5vR_N0Wc5A-nb2oz8IS3hpGBSzqBQf1-iN9BWSwU130_assertion wasDerivedFrom befree-2016 NP871755.RAlXW5vR_N0Wc5A-nb2oz8IS3hpGBSzqBQf1-iN9BWSwU130_provenance.
- NP871755.RAlXW5vR_N0Wc5A-nb2oz8IS3hpGBSzqBQf1-iN9BWSwU130_assertion wasGeneratedBy ECO_0000203 NP871755.RAlXW5vR_N0Wc5A-nb2oz8IS3hpGBSzqBQf1-iN9BWSwU130_provenance.