Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP255337.RALVJV2FmGUMSg65Dx--gpopwovafRNqOPxKtc0cBjB0E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP255337.RALVJV2FmGUMSg65Dx--gpopwovafRNqOPxKtc0cBjB0E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP255337.RALVJV2FmGUMSg65Dx--gpopwovafRNqOPxKtc0cBjB0E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP255337.RALVJV2FmGUMSg65Dx--gpopwovafRNqOPxKtc0cBjB0E130_provenance.
- NP255337.RALVJV2FmGUMSg65Dx--gpopwovafRNqOPxKtc0cBjB0E130_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." NP255337.RALVJV2FmGUMSg65Dx--gpopwovafRNqOPxKtc0cBjB0E130_provenance.
- NP255337.RALVJV2FmGUMSg65Dx--gpopwovafRNqOPxKtc0cBjB0E130_assertion evidence source_evidence_literature NP255337.RALVJV2FmGUMSg65Dx--gpopwovafRNqOPxKtc0cBjB0E130_provenance.
- NP255337.RALVJV2FmGUMSg65Dx--gpopwovafRNqOPxKtc0cBjB0E130_assertion SIO_000772 10373324 NP255337.RALVJV2FmGUMSg65Dx--gpopwovafRNqOPxKtc0cBjB0E130_provenance.
- NP255337.RALVJV2FmGUMSg65Dx--gpopwovafRNqOPxKtc0cBjB0E130_assertion wasDerivedFrom befree-2016 NP255337.RALVJV2FmGUMSg65Dx--gpopwovafRNqOPxKtc0cBjB0E130_provenance.
- NP255337.RALVJV2FmGUMSg65Dx--gpopwovafRNqOPxKtc0cBjB0E130_assertion wasGeneratedBy ECO_0000203 NP255337.RALVJV2FmGUMSg65Dx--gpopwovafRNqOPxKtc0cBjB0E130_provenance.
- befree-2016 importedOn "2016-02-19" NP255337.RALVJV2FmGUMSg65Dx--gpopwovafRNqOPxKtc0cBjB0E130_provenance.