Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP23991.RA3i87SyrKNqelu7WPjej0PLgFwR951DSUwXU3i8O20aY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP23991.RA3i87SyrKNqelu7WPjej0PLgFwR951DSUwXU3i8O20aY130_assertion type Assertion NP23991.RA3i87SyrKNqelu7WPjej0PLgFwR951DSUwXU3i8O20aY130_head.
- NP23991.RA3i87SyrKNqelu7WPjej0PLgFwR951DSUwXU3i8O20aY130_assertion description "[Frontorhiny, a distinctive presentation of frontonasal dysplasia caused by recessive mutations in the ALX3 homeobox gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP23991.RA3i87SyrKNqelu7WPjej0PLgFwR951DSUwXU3i8O20aY130_provenance.
- NP23991.RA3i87SyrKNqelu7WPjej0PLgFwR951DSUwXU3i8O20aY130_assertion evidence source_evidence_curated NP23991.RA3i87SyrKNqelu7WPjej0PLgFwR951DSUwXU3i8O20aY130_provenance.
- NP23991.RA3i87SyrKNqelu7WPjej0PLgFwR951DSUwXU3i8O20aY130_assertion SIO_000772 19409524 NP23991.RA3i87SyrKNqelu7WPjej0PLgFwR951DSUwXU3i8O20aY130_provenance.
- NP23991.RA3i87SyrKNqelu7WPjej0PLgFwR951DSUwXU3i8O20aY130_assertion wasDerivedFrom ctd_human-2016 NP23991.RA3i87SyrKNqelu7WPjej0PLgFwR951DSUwXU3i8O20aY130_provenance.
- NP23991.RA3i87SyrKNqelu7WPjej0PLgFwR951DSUwXU3i8O20aY130_assertion wasGeneratedBy ECO_0000218 NP23991.RA3i87SyrKNqelu7WPjej0PLgFwR951DSUwXU3i8O20aY130_provenance.