Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP365843.RAPQLHT6kDnCZnxDVf67H0lgGtxEkyDjVbhGd9UoMJnkc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP365843.RAPQLHT6kDnCZnxDVf67H0lgGtxEkyDjVbhGd9UoMJnkc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP365843.RAPQLHT6kDnCZnxDVf67H0lgGtxEkyDjVbhGd9UoMJnkc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP365843.RAPQLHT6kDnCZnxDVf67H0lgGtxEkyDjVbhGd9UoMJnkc130_provenance.
- NP365843.RAPQLHT6kDnCZnxDVf67H0lgGtxEkyDjVbhGd9UoMJnkc130_assertion description "[Furthermore, there is strong evidence against linkage to two Hirschsprung disease (a condition that can cosegregate with neuroblastoma) susceptibility genes, RET and EDNRB.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP365843.RAPQLHT6kDnCZnxDVf67H0lgGtxEkyDjVbhGd9UoMJnkc130_provenance.
- NP365843.RAPQLHT6kDnCZnxDVf67H0lgGtxEkyDjVbhGd9UoMJnkc130_assertion evidence source_evidence_literature NP365843.RAPQLHT6kDnCZnxDVf67H0lgGtxEkyDjVbhGd9UoMJnkc130_provenance.
- NP365843.RAPQLHT6kDnCZnxDVf67H0lgGtxEkyDjVbhGd9UoMJnkc130_assertion SIO_000772 8758905 NP365843.RAPQLHT6kDnCZnxDVf67H0lgGtxEkyDjVbhGd9UoMJnkc130_provenance.
- NP365843.RAPQLHT6kDnCZnxDVf67H0lgGtxEkyDjVbhGd9UoMJnkc130_assertion wasDerivedFrom befree-20150227 NP365843.RAPQLHT6kDnCZnxDVf67H0lgGtxEkyDjVbhGd9UoMJnkc130_provenance.
- NP365843.RAPQLHT6kDnCZnxDVf67H0lgGtxEkyDjVbhGd9UoMJnkc130_assertion wasGeneratedBy ECO_0000203 NP365843.RAPQLHT6kDnCZnxDVf67H0lgGtxEkyDjVbhGd9UoMJnkc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP365843.RAPQLHT6kDnCZnxDVf67H0lgGtxEkyDjVbhGd9UoMJnkc130_provenance.