Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP23088.RA0P02B-chH6yVtKXFUNbO137QbFRnxTWZmxrm6YnAaVg130_assertion> ?p ?o ?g. }
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- NP23088.RA0P02B-chH6yVtKXFUNbO137QbFRnxTWZmxrm6YnAaVg130_assertion type Assertion NP23088.RA0P02B-chH6yVtKXFUNbO137QbFRnxTWZmxrm6YnAaVg130_head.
- NP23088.RA0P02B-chH6yVtKXFUNbO137QbFRnxTWZmxrm6YnAaVg130_assertion description "[TBX15 mutations cause craniofacial dysmorphism, hypoplasia of scapula and pelvis, and short stature in Cousin syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP23088.RA0P02B-chH6yVtKXFUNbO137QbFRnxTWZmxrm6YnAaVg130_provenance.
- NP23088.RA0P02B-chH6yVtKXFUNbO137QbFRnxTWZmxrm6YnAaVg130_assertion evidence source_evidence_curated NP23088.RA0P02B-chH6yVtKXFUNbO137QbFRnxTWZmxrm6YnAaVg130_provenance.
- NP23088.RA0P02B-chH6yVtKXFUNbO137QbFRnxTWZmxrm6YnAaVg130_assertion SIO_000772 19068278 NP23088.RA0P02B-chH6yVtKXFUNbO137QbFRnxTWZmxrm6YnAaVg130_provenance.
- NP23088.RA0P02B-chH6yVtKXFUNbO137QbFRnxTWZmxrm6YnAaVg130_assertion wasDerivedFrom ctd_human-2016 NP23088.RA0P02B-chH6yVtKXFUNbO137QbFRnxTWZmxrm6YnAaVg130_provenance.
- NP23088.RA0P02B-chH6yVtKXFUNbO137QbFRnxTWZmxrm6YnAaVg130_assertion wasGeneratedBy ECO_0000218 NP23088.RA0P02B-chH6yVtKXFUNbO137QbFRnxTWZmxrm6YnAaVg130_provenance.