Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP765338.RAhTiyL8ab8fLXKRcT4ICmyK805J9EU-SgIHeA2VaoCrM130_assertion> ?p ?o ?g. }
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- NP765338.RAhTiyL8ab8fLXKRcT4ICmyK805J9EU-SgIHeA2VaoCrM130_assertion type Assertion NP765338.RAhTiyL8ab8fLXKRcT4ICmyK805J9EU-SgIHeA2VaoCrM130_head.
- 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.