Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP325217.RAVDnDzESqmLLwthYqAYo8I87dhXltWQhP7Nm74W9vQik130_assertion> ?p ?o ?g. }
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- NP325217.RAVDnDzESqmLLwthYqAYo8I87dhXltWQhP7Nm74W9vQik130_assertion type Assertion NP325217.RAVDnDzESqmLLwthYqAYo8I87dhXltWQhP7Nm74W9vQik130_head.
- NP325217.RAVDnDzESqmLLwthYqAYo8I87dhXltWQhP7Nm74W9vQik130_assertion wasGeneratedBy ECO_0000203 NP325217.RAVDnDzESqmLLwthYqAYo8I87dhXltWQhP7Nm74W9vQik130_provenance.
- NP325217.RAVDnDzESqmLLwthYqAYo8I87dhXltWQhP7Nm74W9vQik130_assertion wasDerivedFrom befree-20140225 NP325217.RAVDnDzESqmLLwthYqAYo8I87dhXltWQhP7Nm74W9vQik130_provenance.
- NP325217.RAVDnDzESqmLLwthYqAYo8I87dhXltWQhP7Nm74W9vQik130_assertion SIO_000772 11369620 NP325217.RAVDnDzESqmLLwthYqAYo8I87dhXltWQhP7Nm74W9vQik130_provenance.
- NP325217.RAVDnDzESqmLLwthYqAYo8I87dhXltWQhP7Nm74W9vQik130_assertion evidence source_evidence_literature NP325217.RAVDnDzESqmLLwthYqAYo8I87dhXltWQhP7Nm74W9vQik130_provenance.
- NP325217.RAVDnDzESqmLLwthYqAYo8I87dhXltWQhP7Nm74W9vQik130_assertion description "[Pyrimidine 5' nucleotidase (P5'N-1) deficiency is an autosomal recessive condition causing hemolytic anemia characterized by marked basophilic stippling and the accumulation of high concentrations of pyrimidine nucleotides within the erythrocyte.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP325217.RAVDnDzESqmLLwthYqAYo8I87dhXltWQhP7Nm74W9vQik130_provenance.