Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP9533.RAonGv5OLuj8e09ApDoityg2bLyPTknV7112VvtowIDdU130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP9533.RAonGv5OLuj8e09ApDoityg2bLyPTknV7112VvtowIDdU130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP9533.RAonGv5OLuj8e09ApDoityg2bLyPTknV7112VvtowIDdU130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP9533.RAonGv5OLuj8e09ApDoityg2bLyPTknV7112VvtowIDdU130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP9533.RAonGv5OLuj8e09ApDoityg2bLyPTknV7112VvtowIDdU130_provenance.
- NP9533.RAonGv5OLuj8e09ApDoityg2bLyPTknV7112VvtowIDdU130_assertion wasGeneratedBy ECO_0000218 NP9533.RAonGv5OLuj8e09ApDoityg2bLyPTknV7112VvtowIDdU130_provenance.
- NP9533.RAonGv5OLuj8e09ApDoityg2bLyPTknV7112VvtowIDdU130_assertion wasDerivedFrom uniprot-2016 NP9533.RAonGv5OLuj8e09ApDoityg2bLyPTknV7112VvtowIDdU130_provenance.
- NP9533.RAonGv5OLuj8e09ApDoityg2bLyPTknV7112VvtowIDdU130_assertion SIO_000772 9359047 NP9533.RAonGv5OLuj8e09ApDoityg2bLyPTknV7112VvtowIDdU130_provenance.
- NP9533.RAonGv5OLuj8e09ApDoityg2bLyPTknV7112VvtowIDdU130_assertion evidence source_evidence_curated NP9533.RAonGv5OLuj8e09ApDoityg2bLyPTknV7112VvtowIDdU130_provenance.
- NP9533.RAonGv5OLuj8e09ApDoityg2bLyPTknV7112VvtowIDdU130_assertion description "[Endothelin-3 gene mutations in isolated and syndromic Hirschsprung disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP9533.RAonGv5OLuj8e09ApDoityg2bLyPTknV7112VvtowIDdU130_provenance.