Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP425149.RAfRRuNoflaqXQyilOwxEPBNabQAVZkb4LkqE1zX2yIIg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP425149.RAfRRuNoflaqXQyilOwxEPBNabQAVZkb4LkqE1zX2yIIg130_assertion type Assertion NP425149.RAfRRuNoflaqXQyilOwxEPBNabQAVZkb4LkqE1zX2yIIg130_head.
- NP425149.RAfRRuNoflaqXQyilOwxEPBNabQAVZkb4LkqE1zX2yIIg130_assertion description "[Mutations in the zinc finger transcription factor ZIC3 cause X-linked heterotaxy and have also been identified in patients with isolated congenital heart disease (CHD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP425149.RAfRRuNoflaqXQyilOwxEPBNabQAVZkb4LkqE1zX2yIIg130_provenance.
- NP425149.RAfRRuNoflaqXQyilOwxEPBNabQAVZkb4LkqE1zX2yIIg130_assertion evidence source_evidence_literature NP425149.RAfRRuNoflaqXQyilOwxEPBNabQAVZkb4LkqE1zX2yIIg130_provenance.
- NP425149.RAfRRuNoflaqXQyilOwxEPBNabQAVZkb4LkqE1zX2yIIg130_assertion SIO_000772 14681828 NP425149.RAfRRuNoflaqXQyilOwxEPBNabQAVZkb4LkqE1zX2yIIg130_provenance.
- NP425149.RAfRRuNoflaqXQyilOwxEPBNabQAVZkb4LkqE1zX2yIIg130_assertion wasDerivedFrom befree-2016 NP425149.RAfRRuNoflaqXQyilOwxEPBNabQAVZkb4LkqE1zX2yIIg130_provenance.
- NP425149.RAfRRuNoflaqXQyilOwxEPBNabQAVZkb4LkqE1zX2yIIg130_assertion wasGeneratedBy ECO_0000203 NP425149.RAfRRuNoflaqXQyilOwxEPBNabQAVZkb4LkqE1zX2yIIg130_provenance.