Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP393868.RA9TdxqpatQBL0EduqzU-CNfx66q5oskeqzqiOei2I4GU130_assertion> ?p ?o ?g. }
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- NP393868.RA9TdxqpatQBL0EduqzU-CNfx66q5oskeqzqiOei2I4GU130_assertion type Assertion NP393868.RA9TdxqpatQBL0EduqzU-CNfx66q5oskeqzqiOei2I4GU130_head.
- NP393868.RA9TdxqpatQBL0EduqzU-CNfx66q5oskeqzqiOei2I4GU130_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." NP393868.RA9TdxqpatQBL0EduqzU-CNfx66q5oskeqzqiOei2I4GU130_provenance.
- NP393868.RA9TdxqpatQBL0EduqzU-CNfx66q5oskeqzqiOei2I4GU130_assertion evidence source_evidence_literature NP393868.RA9TdxqpatQBL0EduqzU-CNfx66q5oskeqzqiOei2I4GU130_provenance.
- NP393868.RA9TdxqpatQBL0EduqzU-CNfx66q5oskeqzqiOei2I4GU130_assertion SIO_000772 11196105 NP393868.RA9TdxqpatQBL0EduqzU-CNfx66q5oskeqzqiOei2I4GU130_provenance.
- NP393868.RA9TdxqpatQBL0EduqzU-CNfx66q5oskeqzqiOei2I4GU130_assertion wasDerivedFrom befree-20150227 NP393868.RA9TdxqpatQBL0EduqzU-CNfx66q5oskeqzqiOei2I4GU130_provenance.
- NP393868.RA9TdxqpatQBL0EduqzU-CNfx66q5oskeqzqiOei2I4GU130_assertion wasGeneratedBy ECO_0000203 NP393868.RA9TdxqpatQBL0EduqzU-CNfx66q5oskeqzqiOei2I4GU130_provenance.