Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP393841.RA3SniIJc4rm3LQNGS8c7CPu17QvSbguFUYsA3bViOaqg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP393841.RA3SniIJc4rm3LQNGS8c7CPu17QvSbguFUYsA3bViOaqg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP393841.RA3SniIJc4rm3LQNGS8c7CPu17QvSbguFUYsA3bViOaqg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP393841.RA3SniIJc4rm3LQNGS8c7CPu17QvSbguFUYsA3bViOaqg130_provenance.
- NP393841.RA3SniIJc4rm3LQNGS8c7CPu17QvSbguFUYsA3bViOaqg130_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." NP393841.RA3SniIJc4rm3LQNGS8c7CPu17QvSbguFUYsA3bViOaqg130_provenance.
- NP393841.RA3SniIJc4rm3LQNGS8c7CPu17QvSbguFUYsA3bViOaqg130_assertion evidence source_evidence_literature NP393841.RA3SniIJc4rm3LQNGS8c7CPu17QvSbguFUYsA3bViOaqg130_provenance.
- NP393841.RA3SniIJc4rm3LQNGS8c7CPu17QvSbguFUYsA3bViOaqg130_assertion SIO_000772 11196105 NP393841.RA3SniIJc4rm3LQNGS8c7CPu17QvSbguFUYsA3bViOaqg130_provenance.
- NP393841.RA3SniIJc4rm3LQNGS8c7CPu17QvSbguFUYsA3bViOaqg130_assertion wasDerivedFrom befree-20150227 NP393841.RA3SniIJc4rm3LQNGS8c7CPu17QvSbguFUYsA3bViOaqg130_provenance.
- NP393841.RA3SniIJc4rm3LQNGS8c7CPu17QvSbguFUYsA3bViOaqg130_assertion wasGeneratedBy ECO_0000203 NP393841.RA3SniIJc4rm3LQNGS8c7CPu17QvSbguFUYsA3bViOaqg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP393841.RA3SniIJc4rm3LQNGS8c7CPu17QvSbguFUYsA3bViOaqg130_provenance.