Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP5783.RADHvjbSXkNFOet6cfA5KOKnToPrAVvigCWLrylbF-zMs130_assertion> ?p ?o ?g. }
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- NP5783.RADHvjbSXkNFOet6cfA5KOKnToPrAVvigCWLrylbF-zMs130_assertion type Assertion NP5783.RADHvjbSXkNFOet6cfA5KOKnToPrAVvigCWLrylbF-zMs130_head.
- NP5783.RADHvjbSXkNFOet6cfA5KOKnToPrAVvigCWLrylbF-zMs130_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." NP5783.RADHvjbSXkNFOet6cfA5KOKnToPrAVvigCWLrylbF-zMs130_provenance.
- NP5783.RADHvjbSXkNFOet6cfA5KOKnToPrAVvigCWLrylbF-zMs130_assertion evidence source_evidence_curated NP5783.RADHvjbSXkNFOet6cfA5KOKnToPrAVvigCWLrylbF-zMs130_provenance.
- NP5783.RADHvjbSXkNFOet6cfA5KOKnToPrAVvigCWLrylbF-zMs130_assertion SIO_000772 19409524 NP5783.RADHvjbSXkNFOet6cfA5KOKnToPrAVvigCWLrylbF-zMs130_provenance.
- NP5783.RADHvjbSXkNFOet6cfA5KOKnToPrAVvigCWLrylbF-zMs130_assertion wasDerivedFrom uniprot-2016 NP5783.RADHvjbSXkNFOet6cfA5KOKnToPrAVvigCWLrylbF-zMs130_provenance.
- NP5783.RADHvjbSXkNFOet6cfA5KOKnToPrAVvigCWLrylbF-zMs130_assertion wasGeneratedBy ECO_0000218 NP5783.RADHvjbSXkNFOet6cfA5KOKnToPrAVvigCWLrylbF-zMs130_provenance.