Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1355602.RAnhC08RwQxoxUEJAi9XrEoO82_9x2GGv4ElVNmbRrMt8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1355602.RAnhC08RwQxoxUEJAi9XrEoO82_9x2GGv4ElVNmbRrMt8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1355602.RAnhC08RwQxoxUEJAi9XrEoO82_9x2GGv4ElVNmbRrMt8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1355602.RAnhC08RwQxoxUEJAi9XrEoO82_9x2GGv4ElVNmbRrMt8130_provenance.
- NP1355602.RAnhC08RwQxoxUEJAi9XrEoO82_9x2GGv4ElVNmbRrMt8130_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." NP1355602.RAnhC08RwQxoxUEJAi9XrEoO82_9x2GGv4ElVNmbRrMt8130_provenance.
- NP1355602.RAnhC08RwQxoxUEJAi9XrEoO82_9x2GGv4ElVNmbRrMt8130_assertion evidence source_evidence_literature NP1355602.RAnhC08RwQxoxUEJAi9XrEoO82_9x2GGv4ElVNmbRrMt8130_provenance.
- NP1355602.RAnhC08RwQxoxUEJAi9XrEoO82_9x2GGv4ElVNmbRrMt8130_assertion SIO_000772 8758905 NP1355602.RAnhC08RwQxoxUEJAi9XrEoO82_9x2GGv4ElVNmbRrMt8130_provenance.
- NP1355602.RAnhC08RwQxoxUEJAi9XrEoO82_9x2GGv4ElVNmbRrMt8130_assertion wasDerivedFrom befree-2016 NP1355602.RAnhC08RwQxoxUEJAi9XrEoO82_9x2GGv4ElVNmbRrMt8130_provenance.
- NP1355602.RAnhC08RwQxoxUEJAi9XrEoO82_9x2GGv4ElVNmbRrMt8130_assertion wasGeneratedBy ECO_0000203 NP1355602.RAnhC08RwQxoxUEJAi9XrEoO82_9x2GGv4ElVNmbRrMt8130_provenance.
- befree-2016 importedOn "2016-02-19" NP1355602.RAnhC08RwQxoxUEJAi9XrEoO82_9x2GGv4ElVNmbRrMt8130_provenance.