Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP775102.RANxcGm9-Qs1YnQoQOkxkdEDdeXXwDBHzl26_CqJqbbFw130_assertion> ?p ?o ?g. }
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- NP775102.RANxcGm9-Qs1YnQoQOkxkdEDdeXXwDBHzl26_CqJqbbFw130_assertion type Assertion NP775102.RANxcGm9-Qs1YnQoQOkxkdEDdeXXwDBHzl26_CqJqbbFw130_head.
- NP775102.RANxcGm9-Qs1YnQoQOkxkdEDdeXXwDBHzl26_CqJqbbFw130_assertion description "[Isolated 3-methylcrotonyl-CoA carboxylase (MCC) deficiency is an autosomal recessive disorder that appears to be the most frequent organic aciduria detected in tandem mass spectrometry (TMS)-based neonatal screening programs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP775102.RANxcGm9-Qs1YnQoQOkxkdEDdeXXwDBHzl26_CqJqbbFw130_provenance.
- NP775102.RANxcGm9-Qs1YnQoQOkxkdEDdeXXwDBHzl26_CqJqbbFw130_assertion evidence source_evidence_literature NP775102.RANxcGm9-Qs1YnQoQOkxkdEDdeXXwDBHzl26_CqJqbbFw130_provenance.
- NP775102.RANxcGm9-Qs1YnQoQOkxkdEDdeXXwDBHzl26_CqJqbbFw130_assertion SIO_000772 16010683 NP775102.RANxcGm9-Qs1YnQoQOkxkdEDdeXXwDBHzl26_CqJqbbFw130_provenance.
- NP775102.RANxcGm9-Qs1YnQoQOkxkdEDdeXXwDBHzl26_CqJqbbFw130_assertion wasDerivedFrom befree-20140225 NP775102.RANxcGm9-Qs1YnQoQOkxkdEDdeXXwDBHzl26_CqJqbbFw130_provenance.
- NP775102.RANxcGm9-Qs1YnQoQOkxkdEDdeXXwDBHzl26_CqJqbbFw130_assertion wasGeneratedBy ECO_0000203 NP775102.RANxcGm9-Qs1YnQoQOkxkdEDdeXXwDBHzl26_CqJqbbFw130_provenance.