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- NP122.RA1-EwlQR8P4oFCSSpGnn3NF4n8MFBM_EHrIabkuzBNjs130_assertion type Assertion NP122.RA1-EwlQR8P4oFCSSpGnn3NF4n8MFBM_EHrIabkuzBNjs130_head.
- NP122.RA1-EwlQR8P4oFCSSpGnn3NF4n8MFBM_EHrIabkuzBNjs130_assertion description "[As in other metabolic disorders, the distinction between `normal` and `disease` in MCAD deficiency is blurring into a spectrum of enzyme deficiency states caused by different mutations in the ACADM gene potentially influenced by factors affecting intracellular protein processing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP122.RA1-EwlQR8P4oFCSSpGnn3NF4n8MFBM_EHrIabkuzBNjs130_provenance.
- NP122.RA1-EwlQR8P4oFCSSpGnn3NF4n8MFBM_EHrIabkuzBNjs130_assertion evidence source_evidence_curated NP122.RA1-EwlQR8P4oFCSSpGnn3NF4n8MFBM_EHrIabkuzBNjs130_provenance.
- NP122.RA1-EwlQR8P4oFCSSpGnn3NF4n8MFBM_EHrIabkuzBNjs130_assertion SIO_000772 11409868 NP122.RA1-EwlQR8P4oFCSSpGnn3NF4n8MFBM_EHrIabkuzBNjs130_provenance.
- NP122.RA1-EwlQR8P4oFCSSpGnn3NF4n8MFBM_EHrIabkuzBNjs130_assertion wasDerivedFrom uniprot-20130724 NP122.RA1-EwlQR8P4oFCSSpGnn3NF4n8MFBM_EHrIabkuzBNjs130_provenance.
- NP122.RA1-EwlQR8P4oFCSSpGnn3NF4n8MFBM_EHrIabkuzBNjs130_assertion wasGeneratedBy ECO_0000218 NP122.RA1-EwlQR8P4oFCSSpGnn3NF4n8MFBM_EHrIabkuzBNjs130_provenance.