Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP9276.RA-ayQK8FjqYnOUce-NwGODc1AriYMCekWXHTmyaeRal0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP9276.RA-ayQK8FjqYnOUce-NwGODc1AriYMCekWXHTmyaeRal0130_assertion type Assertion NP9276.RA-ayQK8FjqYnOUce-NwGODc1AriYMCekWXHTmyaeRal0130_head.
- NP9276.RA-ayQK8FjqYnOUce-NwGODc1AriYMCekWXHTmyaeRal0130_assertion description "[De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP9276.RA-ayQK8FjqYnOUce-NwGODc1AriYMCekWXHTmyaeRal0130_provenance.
- NP9276.RA-ayQK8FjqYnOUce-NwGODc1AriYMCekWXHTmyaeRal0130_assertion evidence source_evidence_curated NP9276.RA-ayQK8FjqYnOUce-NwGODc1AriYMCekWXHTmyaeRal0130_provenance.
- NP9276.RA-ayQK8FjqYnOUce-NwGODc1AriYMCekWXHTmyaeRal0130_assertion SIO_000772 21706002 NP9276.RA-ayQK8FjqYnOUce-NwGODc1AriYMCekWXHTmyaeRal0130_provenance.
- NP9276.RA-ayQK8FjqYnOUce-NwGODc1AriYMCekWXHTmyaeRal0130_assertion wasDerivedFrom ctd_human-20130708 NP9276.RA-ayQK8FjqYnOUce-NwGODc1AriYMCekWXHTmyaeRal0130_provenance.
- NP9276.RA-ayQK8FjqYnOUce-NwGODc1AriYMCekWXHTmyaeRal0130_assertion wasGeneratedBy ECO_0000218 NP9276.RA-ayQK8FjqYnOUce-NwGODc1AriYMCekWXHTmyaeRal0130_provenance.