Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP409369.RA4IjHTSkPLUbCzVE7-h2Q2bemr9OPEN0J4xRfowryOOI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP409369.RA4IjHTSkPLUbCzVE7-h2Q2bemr9OPEN0J4xRfowryOOI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP409369.RA4IjHTSkPLUbCzVE7-h2Q2bemr9OPEN0J4xRfowryOOI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP409369.RA4IjHTSkPLUbCzVE7-h2Q2bemr9OPEN0J4xRfowryOOI130_provenance.
- NP409369.RA4IjHTSkPLUbCzVE7-h2Q2bemr9OPEN0J4xRfowryOOI130_assertion description "[We have searched for mutations in the maleylacetoacetate isomerase gene in four cases of unexplained severe liver failure in infancy with clinical similarities to hereditary tyrosinemia type I (pseudotyrosinemia).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP409369.RA4IjHTSkPLUbCzVE7-h2Q2bemr9OPEN0J4xRfowryOOI130_provenance.
- NP409369.RA4IjHTSkPLUbCzVE7-h2Q2bemr9OPEN0J4xRfowryOOI130_assertion evidence source_evidence_literature NP409369.RA4IjHTSkPLUbCzVE7-h2Q2bemr9OPEN0J4xRfowryOOI130_provenance.
- NP409369.RA4IjHTSkPLUbCzVE7-h2Q2bemr9OPEN0J4xRfowryOOI130_assertion SIO_000772 10373324 NP409369.RA4IjHTSkPLUbCzVE7-h2Q2bemr9OPEN0J4xRfowryOOI130_provenance.
- NP409369.RA4IjHTSkPLUbCzVE7-h2Q2bemr9OPEN0J4xRfowryOOI130_assertion wasDerivedFrom befree-20140225 NP409369.RA4IjHTSkPLUbCzVE7-h2Q2bemr9OPEN0J4xRfowryOOI130_provenance.
- NP409369.RA4IjHTSkPLUbCzVE7-h2Q2bemr9OPEN0J4xRfowryOOI130_assertion wasGeneratedBy ECO_0000203 NP409369.RA4IjHTSkPLUbCzVE7-h2Q2bemr9OPEN0J4xRfowryOOI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP409369.RA4IjHTSkPLUbCzVE7-h2Q2bemr9OPEN0J4xRfowryOOI130_provenance.