Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP878395.RA6zvyBZzmsO2WeQ6E1WuR5KaN5A8ENwBc6ojcTRyxo8I130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP878395.RA6zvyBZzmsO2WeQ6E1WuR5KaN5A8ENwBc6ojcTRyxo8I130_assertion type Assertion NP878395.RA6zvyBZzmsO2WeQ6E1WuR5KaN5A8ENwBc6ojcTRyxo8I130_head.
- NP878395.RA6zvyBZzmsO2WeQ6E1WuR5KaN5A8ENwBc6ojcTRyxo8I130_assertion description "[Oculocutaneous albinism type 2 (OCA2) with homozygous 2.7-kb deletion of the P gene and sickle cell disease in a Cameroonian family. Identification of a common TAG haplotype in the mutated P gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP878395.RA6zvyBZzmsO2WeQ6E1WuR5KaN5A8ENwBc6ojcTRyxo8I130_provenance.
- NP878395.RA6zvyBZzmsO2WeQ6E1WuR5KaN5A8ENwBc6ojcTRyxo8I130_assertion evidence source_evidence_literature NP878395.RA6zvyBZzmsO2WeQ6E1WuR5KaN5A8ENwBc6ojcTRyxo8I130_provenance.
- NP878395.RA6zvyBZzmsO2WeQ6E1WuR5KaN5A8ENwBc6ojcTRyxo8I130_assertion SIO_000772 17767372 NP878395.RA6zvyBZzmsO2WeQ6E1WuR5KaN5A8ENwBc6ojcTRyxo8I130_provenance.
- NP878395.RA6zvyBZzmsO2WeQ6E1WuR5KaN5A8ENwBc6ojcTRyxo8I130_assertion wasDerivedFrom befree-20140225 NP878395.RA6zvyBZzmsO2WeQ6E1WuR5KaN5A8ENwBc6ojcTRyxo8I130_provenance.
- NP878395.RA6zvyBZzmsO2WeQ6E1WuR5KaN5A8ENwBc6ojcTRyxo8I130_assertion wasGeneratedBy ECO_0000203 NP878395.RA6zvyBZzmsO2WeQ6E1WuR5KaN5A8ENwBc6ojcTRyxo8I130_provenance.