Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1414444.RAPMaSA8NcgP08EsIZkyzODMguwAJyNG39DJ5PoOW9HU8#assertion> ?p ?o ?g. }
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- assertion description "[De novo ASXL1 mutations cause Bohring-Opitz syndrome characterized by multiple congenital malformations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion evidence source_evidence_literature provenance.
- assertion SIO_000772 24255920 provenance.
- assertion wasDerivedFrom BEFREE provenance.
- assertion wasGeneratedBy ECO_0000203 provenance.