Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP393836.RAED9KSJ0629gcFp-cuB3NSE1svdNCaWGQYMkNJ6-Pqds130_assertion> ?p ?o ?g. }
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- NP393836.RAED9KSJ0629gcFp-cuB3NSE1svdNCaWGQYMkNJ6-Pqds130_assertion type Assertion NP393836.RAED9KSJ0629gcFp-cuB3NSE1svdNCaWGQYMkNJ6-Pqds130_head.
- NP393836.RAED9KSJ0629gcFp-cuB3NSE1svdNCaWGQYMkNJ6-Pqds130_assertion description "[Tyrosinaemia I (fumarylacetoacetate hydrolase deficiency) is an autosomal recessive inborn error of tyrosine metabolism that produces liver failure in infancy or a more chronic course of liver disease with cirrhosis, often complicated by hepatocellular carcinoma, in childhood or early adolescence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP393836.RAED9KSJ0629gcFp-cuB3NSE1svdNCaWGQYMkNJ6-Pqds130_provenance.
- NP393836.RAED9KSJ0629gcFp-cuB3NSE1svdNCaWGQYMkNJ6-Pqds130_assertion evidence source_evidence_literature NP393836.RAED9KSJ0629gcFp-cuB3NSE1svdNCaWGQYMkNJ6-Pqds130_provenance.
- NP393836.RAED9KSJ0629gcFp-cuB3NSE1svdNCaWGQYMkNJ6-Pqds130_assertion SIO_000772 11196105 NP393836.RAED9KSJ0629gcFp-cuB3NSE1svdNCaWGQYMkNJ6-Pqds130_provenance.
- NP393836.RAED9KSJ0629gcFp-cuB3NSE1svdNCaWGQYMkNJ6-Pqds130_assertion wasDerivedFrom befree-20150227 NP393836.RAED9KSJ0629gcFp-cuB3NSE1svdNCaWGQYMkNJ6-Pqds130_provenance.
- NP393836.RAED9KSJ0629gcFp-cuB3NSE1svdNCaWGQYMkNJ6-Pqds130_assertion wasGeneratedBy ECO_0000203 NP393836.RAED9KSJ0629gcFp-cuB3NSE1svdNCaWGQYMkNJ6-Pqds130_provenance.