Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP192.RAbxiuWQmUBoYFxLbxam5VXauvt2gKIu50kmSQtfGjVVQ130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP192.RAbxiuWQmUBoYFxLbxam5VXauvt2gKIu50kmSQtfGjVVQ130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP192.RAbxiuWQmUBoYFxLbxam5VXauvt2gKIu50kmSQtfGjVVQ130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP192.RAbxiuWQmUBoYFxLbxam5VXauvt2gKIu50kmSQtfGjVVQ130_provenance.
- NP192.RAbxiuWQmUBoYFxLbxam5VXauvt2gKIu50kmSQtfGjVVQ130_assertion description "[Nonsense and temperature-sensitive mutations in PEX13 are the cause of complementation group H of peroxisome biogenesis disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP192.RAbxiuWQmUBoYFxLbxam5VXauvt2gKIu50kmSQtfGjVVQ130_provenance.
- NP192.RAbxiuWQmUBoYFxLbxam5VXauvt2gKIu50kmSQtfGjVVQ130_assertion evidence source_evidence_curated NP192.RAbxiuWQmUBoYFxLbxam5VXauvt2gKIu50kmSQtfGjVVQ130_provenance.
- NP192.RAbxiuWQmUBoYFxLbxam5VXauvt2gKIu50kmSQtfGjVVQ130_assertion SIO_000772 10332040 NP192.RAbxiuWQmUBoYFxLbxam5VXauvt2gKIu50kmSQtfGjVVQ130_provenance.
- NP192.RAbxiuWQmUBoYFxLbxam5VXauvt2gKIu50kmSQtfGjVVQ130_assertion wasDerivedFrom uniprot-2016 NP192.RAbxiuWQmUBoYFxLbxam5VXauvt2gKIu50kmSQtfGjVVQ130_provenance.
- NP192.RAbxiuWQmUBoYFxLbxam5VXauvt2gKIu50kmSQtfGjVVQ130_assertion wasGeneratedBy ECO_0000218 NP192.RAbxiuWQmUBoYFxLbxam5VXauvt2gKIu50kmSQtfGjVVQ130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP192.RAbxiuWQmUBoYFxLbxam5VXauvt2gKIu50kmSQtfGjVVQ130_provenance.