Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP367.RAnxbgQJc5NN62tKpG6m-c6iu0F5UhNwN7IXUviM620O8130_assertion> ?p ?o ?g. }
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- NP367.RAnxbgQJc5NN62tKpG6m-c6iu0F5UhNwN7IXUviM620O8130_assertion type Assertion NP367.RAnxbgQJc5NN62tKpG6m-c6iu0F5UhNwN7IXUviM620O8130_head.
- NP367.RAnxbgQJc5NN62tKpG6m-c6iu0F5UhNwN7IXUviM620O8130_assertion description "[The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP367.RAnxbgQJc5NN62tKpG6m-c6iu0F5UhNwN7IXUviM620O8130_provenance.
- NP367.RAnxbgQJc5NN62tKpG6m-c6iu0F5UhNwN7IXUviM620O8130_assertion evidence source_evidence_curated NP367.RAnxbgQJc5NN62tKpG6m-c6iu0F5UhNwN7IXUviM620O8130_provenance.
- NP367.RAnxbgQJc5NN62tKpG6m-c6iu0F5UhNwN7IXUviM620O8130_assertion SIO_000772 11106354 NP367.RAnxbgQJc5NN62tKpG6m-c6iu0F5UhNwN7IXUviM620O8130_provenance.
- NP367.RAnxbgQJc5NN62tKpG6m-c6iu0F5UhNwN7IXUviM620O8130_assertion wasDerivedFrom uniprot-20130724 NP367.RAnxbgQJc5NN62tKpG6m-c6iu0F5UhNwN7IXUviM620O8130_provenance.
- NP367.RAnxbgQJc5NN62tKpG6m-c6iu0F5UhNwN7IXUviM620O8130_assertion wasGeneratedBy ECO_0000218 NP367.RAnxbgQJc5NN62tKpG6m-c6iu0F5UhNwN7IXUviM620O8130_provenance.