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- NP933507.RAnzYzMSCAr8a56UxnfkoQXwyqHsIc5LK-TKEnxVFX-0U130_assertion type Assertion NP933507.RAnzYzMSCAr8a56UxnfkoQXwyqHsIc5LK-TKEnxVFX-0U130_head.
- NP933507.RAnzYzMSCAr8a56UxnfkoQXwyqHsIc5LK-TKEnxVFX-0U130_assertion description "[Severe erythrocyte adenylate kinase deficiency due to homozygous A-->G substitution at codon 164 of human AK1 gene associated with chronic haemolytic anaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP933507.RAnzYzMSCAr8a56UxnfkoQXwyqHsIc5LK-TKEnxVFX-0U130_provenance.
- NP933507.RAnzYzMSCAr8a56UxnfkoQXwyqHsIc5LK-TKEnxVFX-0U130_assertion evidence source_evidence_literature NP933507.RAnzYzMSCAr8a56UxnfkoQXwyqHsIc5LK-TKEnxVFX-0U130_provenance.
- NP933507.RAnzYzMSCAr8a56UxnfkoQXwyqHsIc5LK-TKEnxVFX-0U130_assertion SIO_000772 9432020 NP933507.RAnzYzMSCAr8a56UxnfkoQXwyqHsIc5LK-TKEnxVFX-0U130_provenance.
- NP933507.RAnzYzMSCAr8a56UxnfkoQXwyqHsIc5LK-TKEnxVFX-0U130_assertion wasDerivedFrom befree-20140225 NP933507.RAnzYzMSCAr8a56UxnfkoQXwyqHsIc5LK-TKEnxVFX-0U130_provenance.
- NP933507.RAnzYzMSCAr8a56UxnfkoQXwyqHsIc5LK-TKEnxVFX-0U130_assertion wasGeneratedBy ECO_0000203 NP933507.RAnzYzMSCAr8a56UxnfkoQXwyqHsIc5LK-TKEnxVFX-0U130_provenance.