Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP644051.RADXyUSbiEIpdQABkDTnA2qnkYaxRBwJyTm5FhH5ERs0A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP644051.RADXyUSbiEIpdQABkDTnA2qnkYaxRBwJyTm5FhH5ERs0A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP644051.RADXyUSbiEIpdQABkDTnA2qnkYaxRBwJyTm5FhH5ERs0A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP644051.RADXyUSbiEIpdQABkDTnA2qnkYaxRBwJyTm5FhH5ERs0A130_provenance.
- NP644051.RADXyUSbiEIpdQABkDTnA2qnkYaxRBwJyTm5FhH5ERs0A130_assertion description "[Patients suffering from the metabolic disease hereditary tyrosinemia type I (HT1), caused by fumarylacetoacetate hydrolase deficiency, have a high risk of developing liver cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP644051.RADXyUSbiEIpdQABkDTnA2qnkYaxRBwJyTm5FhH5ERs0A130_provenance.
- NP644051.RADXyUSbiEIpdQABkDTnA2qnkYaxRBwJyTm5FhH5ERs0A130_assertion evidence source_evidence_literature NP644051.RADXyUSbiEIpdQABkDTnA2qnkYaxRBwJyTm5FhH5ERs0A130_provenance.
- NP644051.RADXyUSbiEIpdQABkDTnA2qnkYaxRBwJyTm5FhH5ERs0A130_assertion SIO_000772 11532983 NP644051.RADXyUSbiEIpdQABkDTnA2qnkYaxRBwJyTm5FhH5ERs0A130_provenance.
- NP644051.RADXyUSbiEIpdQABkDTnA2qnkYaxRBwJyTm5FhH5ERs0A130_assertion wasDerivedFrom befree-20140225 NP644051.RADXyUSbiEIpdQABkDTnA2qnkYaxRBwJyTm5FhH5ERs0A130_provenance.
- NP644051.RADXyUSbiEIpdQABkDTnA2qnkYaxRBwJyTm5FhH5ERs0A130_assertion wasGeneratedBy ECO_0000203 NP644051.RADXyUSbiEIpdQABkDTnA2qnkYaxRBwJyTm5FhH5ERs0A130_provenance.
- befree-20140225 importedOn "2014-02-25" NP644051.RADXyUSbiEIpdQABkDTnA2qnkYaxRBwJyTm5FhH5ERs0A130_provenance.