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- NP632247.RADMAfT064tOyM03bdeioTL3YjsnPpvAL252Pseyhmom4130_assertion type Assertion NP632247.RADMAfT064tOyM03bdeioTL3YjsnPpvAL252Pseyhmom4130_head.
- NP632247.RADMAfT064tOyM03bdeioTL3YjsnPpvAL252Pseyhmom4130_assertion wasGeneratedBy ECO_0000203 NP632247.RADMAfT064tOyM03bdeioTL3YjsnPpvAL252Pseyhmom4130_provenance.
- NP632247.RADMAfT064tOyM03bdeioTL3YjsnPpvAL252Pseyhmom4130_assertion wasDerivedFrom befree-20150227 NP632247.RADMAfT064tOyM03bdeioTL3YjsnPpvAL252Pseyhmom4130_provenance.
- NP632247.RADMAfT064tOyM03bdeioTL3YjsnPpvAL252Pseyhmom4130_assertion SIO_000772 11891694 NP632247.RADMAfT064tOyM03bdeioTL3YjsnPpvAL252Pseyhmom4130_provenance.
- NP632247.RADMAfT064tOyM03bdeioTL3YjsnPpvAL252Pseyhmom4130_assertion evidence source_evidence_literature NP632247.RADMAfT064tOyM03bdeioTL3YjsnPpvAL252Pseyhmom4130_provenance.
- NP632247.RADMAfT064tOyM03bdeioTL3YjsnPpvAL252Pseyhmom4130_assertion description "[A deletion-insertion mutation in the phosphomannomutase 2 gene in an African American patient with congenital disorders of glycosylation-Ia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP632247.RADMAfT064tOyM03bdeioTL3YjsnPpvAL252Pseyhmom4130_provenance.