Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP765338.RAhTiyL8ab8fLXKRcT4ICmyK805J9EU-SgIHeA2VaoCrM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP765338.RAhTiyL8ab8fLXKRcT4ICmyK805J9EU-SgIHeA2VaoCrM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP765338.RAhTiyL8ab8fLXKRcT4ICmyK805J9EU-SgIHeA2VaoCrM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP765338.RAhTiyL8ab8fLXKRcT4ICmyK805J9EU-SgIHeA2VaoCrM130_provenance.
- NP765338.RAhTiyL8ab8fLXKRcT4ICmyK805J9EU-SgIHeA2VaoCrM130_assertion wasGeneratedBy ECO_0000203 NP765338.RAhTiyL8ab8fLXKRcT4ICmyK805J9EU-SgIHeA2VaoCrM130_provenance.
- NP765338.RAhTiyL8ab8fLXKRcT4ICmyK805J9EU-SgIHeA2VaoCrM130_assertion wasDerivedFrom befree-20140225 NP765338.RAhTiyL8ab8fLXKRcT4ICmyK805J9EU-SgIHeA2VaoCrM130_provenance.
- NP765338.RAhTiyL8ab8fLXKRcT4ICmyK805J9EU-SgIHeA2VaoCrM130_assertion SIO_000772 10792313 NP765338.RAhTiyL8ab8fLXKRcT4ICmyK805J9EU-SgIHeA2VaoCrM130_provenance.
- NP765338.RAhTiyL8ab8fLXKRcT4ICmyK805J9EU-SgIHeA2VaoCrM130_assertion evidence source_evidence_literature NP765338.RAhTiyL8ab8fLXKRcT4ICmyK805J9EU-SgIHeA2VaoCrM130_provenance.
- NP765338.RAhTiyL8ab8fLXKRcT4ICmyK805J9EU-SgIHeA2VaoCrM130_assertion description "[However, the similarity between the distal colonic aganglionosis in Hirschsprung disease and that due to EDN3 or EDNRB mutations led to the hypothesis that levels of expression of these genes might be affected in the absence of mutation, thus causing the Hirschsprung disease phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP765338.RAhTiyL8ab8fLXKRcT4ICmyK805J9EU-SgIHeA2VaoCrM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP765338.RAhTiyL8ab8fLXKRcT4ICmyK805J9EU-SgIHeA2VaoCrM130_provenance.