Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP487135.RAqMVMm6BUqsT_WqXm5sqdZdKCKZCC5L3qRorBksxotNo130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP487135.RAqMVMm6BUqsT_WqXm5sqdZdKCKZCC5L3qRorBksxotNo130_assertion type Assertion NP487135.RAqMVMm6BUqsT_WqXm5sqdZdKCKZCC5L3qRorBksxotNo130_head.
- NP487135.RAqMVMm6BUqsT_WqXm5sqdZdKCKZCC5L3qRorBksxotNo130_assertion description "[Longitudinal follow-up revealed that this family has X-linked heterotaxy due to a missense mutation, c.1048A>G(R350G), in the third zinc finger domain of ZIC3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP487135.RAqMVMm6BUqsT_WqXm5sqdZdKCKZCC5L3qRorBksxotNo130_provenance.
- NP487135.RAqMVMm6BUqsT_WqXm5sqdZdKCKZCC5L3qRorBksxotNo130_assertion evidence source_evidence_literature NP487135.RAqMVMm6BUqsT_WqXm5sqdZdKCKZCC5L3qRorBksxotNo130_provenance.
- NP487135.RAqMVMm6BUqsT_WqXm5sqdZdKCKZCC5L3qRorBksxotNo130_assertion SIO_000772 22171628 NP487135.RAqMVMm6BUqsT_WqXm5sqdZdKCKZCC5L3qRorBksxotNo130_provenance.
- NP487135.RAqMVMm6BUqsT_WqXm5sqdZdKCKZCC5L3qRorBksxotNo130_assertion wasDerivedFrom befree-20140225 NP487135.RAqMVMm6BUqsT_WqXm5sqdZdKCKZCC5L3qRorBksxotNo130_provenance.
- NP487135.RAqMVMm6BUqsT_WqXm5sqdZdKCKZCC5L3qRorBksxotNo130_assertion wasGeneratedBy ECO_0000203 NP487135.RAqMVMm6BUqsT_WqXm5sqdZdKCKZCC5L3qRorBksxotNo130_provenance.