Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1004310.RAFI_hW-Dki6K0ivtZMxB36dv1iXUNEEnNmlGCeYZeWOQ130_assertion> ?p ?o ?g. }
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- NP1004310.RAFI_hW-Dki6K0ivtZMxB36dv1iXUNEEnNmlGCeYZeWOQ130_assertion type Assertion NP1004310.RAFI_hW-Dki6K0ivtZMxB36dv1iXUNEEnNmlGCeYZeWOQ130_head.
- NP1004310.RAFI_hW-Dki6K0ivtZMxB36dv1iXUNEEnNmlGCeYZeWOQ130_assertion description "[Here, by a combined approach of homozygozity mapping and exome ciliary sequencing, we identified truncating TCTN3 mutations as the cause of an extreme form of�OFD associated with bone dysplasia, tibial defect, cystic kidneys, and brain anomalies (OFD IV, Mohr-Majewski syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1004310.RAFI_hW-Dki6K0ivtZMxB36dv1iXUNEEnNmlGCeYZeWOQ130_provenance.
- NP1004310.RAFI_hW-Dki6K0ivtZMxB36dv1iXUNEEnNmlGCeYZeWOQ130_assertion evidence source_evidence_literature NP1004310.RAFI_hW-Dki6K0ivtZMxB36dv1iXUNEEnNmlGCeYZeWOQ130_provenance.
- NP1004310.RAFI_hW-Dki6K0ivtZMxB36dv1iXUNEEnNmlGCeYZeWOQ130_assertion SIO_000772 22883145 NP1004310.RAFI_hW-Dki6K0ivtZMxB36dv1iXUNEEnNmlGCeYZeWOQ130_provenance.
- NP1004310.RAFI_hW-Dki6K0ivtZMxB36dv1iXUNEEnNmlGCeYZeWOQ130_assertion wasDerivedFrom befree-2016 NP1004310.RAFI_hW-Dki6K0ivtZMxB36dv1iXUNEEnNmlGCeYZeWOQ130_provenance.
- NP1004310.RAFI_hW-Dki6K0ivtZMxB36dv1iXUNEEnNmlGCeYZeWOQ130_assertion wasGeneratedBy ECO_0000203 NP1004310.RAFI_hW-Dki6K0ivtZMxB36dv1iXUNEEnNmlGCeYZeWOQ130_provenance.