Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP316913.RA8avd9uLWf9PqcEA9Ean8Gs7GATEYIOi1wPADcZOG0SA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP316913.RA8avd9uLWf9PqcEA9Ean8Gs7GATEYIOi1wPADcZOG0SA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP316913.RA8avd9uLWf9PqcEA9Ean8Gs7GATEYIOi1wPADcZOG0SA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP316913.RA8avd9uLWf9PqcEA9Ean8Gs7GATEYIOi1wPADcZOG0SA130_provenance.
- NP316913.RA8avd9uLWf9PqcEA9Ean8Gs7GATEYIOi1wPADcZOG0SA130_assertion description "[Point nucleotidic changes in both the RET proto-oncogene and the endothelin-B receptor gene in a Hirschsprung disease patient associated with Down syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316913.RA8avd9uLWf9PqcEA9Ean8Gs7GATEYIOi1wPADcZOG0SA130_provenance.
- NP316913.RA8avd9uLWf9PqcEA9Ean8Gs7GATEYIOi1wPADcZOG0SA130_assertion evidence source_evidence_literature NP316913.RA8avd9uLWf9PqcEA9Ean8Gs7GATEYIOi1wPADcZOG0SA130_provenance.
- NP316913.RA8avd9uLWf9PqcEA9Ean8Gs7GATEYIOi1wPADcZOG0SA130_assertion SIO_000772 10458491 NP316913.RA8avd9uLWf9PqcEA9Ean8Gs7GATEYIOi1wPADcZOG0SA130_provenance.
- NP316913.RA8avd9uLWf9PqcEA9Ean8Gs7GATEYIOi1wPADcZOG0SA130_assertion wasDerivedFrom befree-20140225 NP316913.RA8avd9uLWf9PqcEA9Ean8Gs7GATEYIOi1wPADcZOG0SA130_provenance.
- NP316913.RA8avd9uLWf9PqcEA9Ean8Gs7GATEYIOi1wPADcZOG0SA130_assertion wasGeneratedBy ECO_0000203 NP316913.RA8avd9uLWf9PqcEA9Ean8Gs7GATEYIOi1wPADcZOG0SA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP316913.RA8avd9uLWf9PqcEA9Ean8Gs7GATEYIOi1wPADcZOG0SA130_provenance.