Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP386783.RACPyaO5TsUvxpbECCE-X2FENE9C4OZTye3H7S78rZk1Q130_assertion> ?p ?o ?g. }
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- NP386783.RACPyaO5TsUvxpbECCE-X2FENE9C4OZTye3H7S78rZk1Q130_assertion type Assertion NP386783.RACPyaO5TsUvxpbECCE-X2FENE9C4OZTye3H7S78rZk1Q130_head.
- NP386783.RACPyaO5TsUvxpbECCE-X2FENE9C4OZTye3H7S78rZk1Q130_assertion description "[Analysis of the CRELD1 gene from individuals with non-trisomy 21-associated AVSD identified heterozygous missense mutations in nearly 6% of this population, including mutations in isolated AVSD and AVSD associated with heterotaxy syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP386783.RACPyaO5TsUvxpbECCE-X2FENE9C4OZTye3H7S78rZk1Q130_provenance.
- NP386783.RACPyaO5TsUvxpbECCE-X2FENE9C4OZTye3H7S78rZk1Q130_assertion evidence source_evidence_literature NP386783.RACPyaO5TsUvxpbECCE-X2FENE9C4OZTye3H7S78rZk1Q130_provenance.
- NP386783.RACPyaO5TsUvxpbECCE-X2FENE9C4OZTye3H7S78rZk1Q130_assertion SIO_000772 12632326 NP386783.RACPyaO5TsUvxpbECCE-X2FENE9C4OZTye3H7S78rZk1Q130_provenance.
- NP386783.RACPyaO5TsUvxpbECCE-X2FENE9C4OZTye3H7S78rZk1Q130_assertion wasDerivedFrom befree-2016 NP386783.RACPyaO5TsUvxpbECCE-X2FENE9C4OZTye3H7S78rZk1Q130_provenance.
- NP386783.RACPyaO5TsUvxpbECCE-X2FENE9C4OZTye3H7S78rZk1Q130_assertion wasGeneratedBy ECO_0000203 NP386783.RACPyaO5TsUvxpbECCE-X2FENE9C4OZTye3H7S78rZk1Q130_provenance.