Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP182744.RAaLaNoxhZ-lV0PWOkdus157C5LSc_zH8yXEIMgt76MNY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP182744.RAaLaNoxhZ-lV0PWOkdus157C5LSc_zH8yXEIMgt76MNY130_assertion type Assertion NP182744.RAaLaNoxhZ-lV0PWOkdus157C5LSc_zH8yXEIMgt76MNY130_head.
- NP182744.RAaLaNoxhZ-lV0PWOkdus157C5LSc_zH8yXEIMgt76MNY130_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." NP182744.RAaLaNoxhZ-lV0PWOkdus157C5LSc_zH8yXEIMgt76MNY130_provenance.
- NP182744.RAaLaNoxhZ-lV0PWOkdus157C5LSc_zH8yXEIMgt76MNY130_assertion evidence source_evidence_literature NP182744.RAaLaNoxhZ-lV0PWOkdus157C5LSc_zH8yXEIMgt76MNY130_provenance.
- NP182744.RAaLaNoxhZ-lV0PWOkdus157C5LSc_zH8yXEIMgt76MNY130_assertion SIO_000772 12632326 NP182744.RAaLaNoxhZ-lV0PWOkdus157C5LSc_zH8yXEIMgt76MNY130_provenance.
- NP182744.RAaLaNoxhZ-lV0PWOkdus157C5LSc_zH8yXEIMgt76MNY130_assertion wasDerivedFrom befree-20140225 NP182744.RAaLaNoxhZ-lV0PWOkdus157C5LSc_zH8yXEIMgt76MNY130_provenance.
- NP182744.RAaLaNoxhZ-lV0PWOkdus157C5LSc_zH8yXEIMgt76MNY130_assertion wasGeneratedBy ECO_0000203 NP182744.RAaLaNoxhZ-lV0PWOkdus157C5LSc_zH8yXEIMgt76MNY130_provenance.