Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP221300.RAhgVYIuVmz_j1uF-wi0rdrHb6c1NWFKwFjFMlLPAqJxg130_assertion> ?p ?o ?g. }
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- NP221300.RAhgVYIuVmz_j1uF-wi0rdrHb6c1NWFKwFjFMlLPAqJxg130_assertion type Assertion NP221300.RAhgVYIuVmz_j1uF-wi0rdrHb6c1NWFKwFjFMlLPAqJxg130_head.
- NP221300.RAhgVYIuVmz_j1uF-wi0rdrHb6c1NWFKwFjFMlLPAqJxg130_assertion wasGeneratedBy ECO_0000203 NP221300.RAhgVYIuVmz_j1uF-wi0rdrHb6c1NWFKwFjFMlLPAqJxg130_provenance.
- NP221300.RAhgVYIuVmz_j1uF-wi0rdrHb6c1NWFKwFjFMlLPAqJxg130_assertion wasDerivedFrom befree-20150227 NP221300.RAhgVYIuVmz_j1uF-wi0rdrHb6c1NWFKwFjFMlLPAqJxg130_provenance.
- NP221300.RAhgVYIuVmz_j1uF-wi0rdrHb6c1NWFKwFjFMlLPAqJxg130_assertion SIO_000772 11369620 NP221300.RAhgVYIuVmz_j1uF-wi0rdrHb6c1NWFKwFjFMlLPAqJxg130_provenance.
- NP221300.RAhgVYIuVmz_j1uF-wi0rdrHb6c1NWFKwFjFMlLPAqJxg130_assertion evidence source_evidence_literature NP221300.RAhgVYIuVmz_j1uF-wi0rdrHb6c1NWFKwFjFMlLPAqJxg130_provenance.
- NP221300.RAhgVYIuVmz_j1uF-wi0rdrHb6c1NWFKwFjFMlLPAqJxg130_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." NP221300.RAhgVYIuVmz_j1uF-wi0rdrHb6c1NWFKwFjFMlLPAqJxg130_provenance.