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- NP307957.RAUx6ej03GAhs1pIzcoCYEnudw5GK3-BBEr02jZSlx3YY130_assertion type Assertion NP307957.RAUx6ej03GAhs1pIzcoCYEnudw5GK3-BBEr02jZSlx3YY130_head.
- NP307957.RAUx6ej03GAhs1pIzcoCYEnudw5GK3-BBEr02jZSlx3YY130_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." NP307957.RAUx6ej03GAhs1pIzcoCYEnudw5GK3-BBEr02jZSlx3YY130_provenance.
- NP307957.RAUx6ej03GAhs1pIzcoCYEnudw5GK3-BBEr02jZSlx3YY130_assertion evidence source_evidence_literature NP307957.RAUx6ej03GAhs1pIzcoCYEnudw5GK3-BBEr02jZSlx3YY130_provenance.
- NP307957.RAUx6ej03GAhs1pIzcoCYEnudw5GK3-BBEr02jZSlx3YY130_assertion SIO_000772 11196105 NP307957.RAUx6ej03GAhs1pIzcoCYEnudw5GK3-BBEr02jZSlx3YY130_provenance.
- NP307957.RAUx6ej03GAhs1pIzcoCYEnudw5GK3-BBEr02jZSlx3YY130_assertion wasDerivedFrom befree-2016 NP307957.RAUx6ej03GAhs1pIzcoCYEnudw5GK3-BBEr02jZSlx3YY130_provenance.
- NP307957.RAUx6ej03GAhs1pIzcoCYEnudw5GK3-BBEr02jZSlx3YY130_assertion wasGeneratedBy ECO_0000203 NP307957.RAUx6ej03GAhs1pIzcoCYEnudw5GK3-BBEr02jZSlx3YY130_provenance.