Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP19234.RAwwfe9hiK5W0Y1a_mUyDvd_hy1nMQlIpWmHf2d2BxdeM130_assertion> ?p ?o ?g. }
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- NP19234.RAwwfe9hiK5W0Y1a_mUyDvd_hy1nMQlIpWmHf2d2BxdeM130_assertion type Assertion NP19234.RAwwfe9hiK5W0Y1a_mUyDvd_hy1nMQlIpWmHf2d2BxdeM130_head.
- NP19234.RAwwfe9hiK5W0Y1a_mUyDvd_hy1nMQlIpWmHf2d2BxdeM130_assertion wasGeneratedBy ECO_0000218 NP19234.RAwwfe9hiK5W0Y1a_mUyDvd_hy1nMQlIpWmHf2d2BxdeM130_provenance.
- NP19234.RAwwfe9hiK5W0Y1a_mUyDvd_hy1nMQlIpWmHf2d2BxdeM130_assertion wasDerivedFrom ctd_human-20130708 NP19234.RAwwfe9hiK5W0Y1a_mUyDvd_hy1nMQlIpWmHf2d2BxdeM130_provenance.
- NP19234.RAwwfe9hiK5W0Y1a_mUyDvd_hy1nMQlIpWmHf2d2BxdeM130_assertion SIO_000772 20493458 NP19234.RAwwfe9hiK5W0Y1a_mUyDvd_hy1nMQlIpWmHf2d2BxdeM130_provenance.
- NP19234.RAwwfe9hiK5W0Y1a_mUyDvd_hy1nMQlIpWmHf2d2BxdeM130_assertion evidence source_evidence_curated NP19234.RAwwfe9hiK5W0Y1a_mUyDvd_hy1nMQlIpWmHf2d2BxdeM130_provenance.
- NP19234.RAwwfe9hiK5W0Y1a_mUyDvd_hy1nMQlIpWmHf2d2BxdeM130_assertion description "[Because not all of our patients harbored mutations in IFT122, CED seems to be genetically heterogeneous.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP19234.RAwwfe9hiK5W0Y1a_mUyDvd_hy1nMQlIpWmHf2d2BxdeM130_provenance.