Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP307958.RAkhegBwns_lja-UQ34UriRNiefYvBRfYMKeH4iDHWQlI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP307958.RAkhegBwns_lja-UQ34UriRNiefYvBRfYMKeH4iDHWQlI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP307958.RAkhegBwns_lja-UQ34UriRNiefYvBRfYMKeH4iDHWQlI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP307958.RAkhegBwns_lja-UQ34UriRNiefYvBRfYMKeH4iDHWQlI130_provenance.
- NP307958.RAkhegBwns_lja-UQ34UriRNiefYvBRfYMKeH4iDHWQlI130_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." NP307958.RAkhegBwns_lja-UQ34UriRNiefYvBRfYMKeH4iDHWQlI130_provenance.
- NP307958.RAkhegBwns_lja-UQ34UriRNiefYvBRfYMKeH4iDHWQlI130_assertion evidence source_evidence_literature NP307958.RAkhegBwns_lja-UQ34UriRNiefYvBRfYMKeH4iDHWQlI130_provenance.
- NP307958.RAkhegBwns_lja-UQ34UriRNiefYvBRfYMKeH4iDHWQlI130_assertion SIO_000772 11196105 NP307958.RAkhegBwns_lja-UQ34UriRNiefYvBRfYMKeH4iDHWQlI130_provenance.
- NP307958.RAkhegBwns_lja-UQ34UriRNiefYvBRfYMKeH4iDHWQlI130_assertion wasDerivedFrom befree-2016 NP307958.RAkhegBwns_lja-UQ34UriRNiefYvBRfYMKeH4iDHWQlI130_provenance.
- NP307958.RAkhegBwns_lja-UQ34UriRNiefYvBRfYMKeH4iDHWQlI130_assertion wasGeneratedBy ECO_0000203 NP307958.RAkhegBwns_lja-UQ34UriRNiefYvBRfYMKeH4iDHWQlI130_provenance.
- befree-2016 importedOn "2016-02-19" NP307958.RAkhegBwns_lja-UQ34UriRNiefYvBRfYMKeH4iDHWQlI130_provenance.