Matches in Nanopublications for { ?s ?p "[Rare putative mutations in the PCP genes VANGL2, SCRIB, DACT1, and CELSR1 cumulatively contributed to over 20% of cases with craniorachischisis, a rare defect; no contributing variants were found for PRICKLE1 or PTK7.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP827863.RAXlp6qPGs9rgOP6Z7kflY2vLWoaMrAFMnCVh-OG0O1L4130_assertion description "[Rare putative mutations in the PCP genes VANGL2, SCRIB, DACT1, and CELSR1 cumulatively contributed to over 20% of cases with craniorachischisis, a rare defect; no contributing variants were found for PRICKLE1 or PTK7.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP827863.RAXlp6qPGs9rgOP6Z7kflY2vLWoaMrAFMnCVh-OG0O1L4130_provenance.
- NP1016690.RAy06Vc3XjCpyBY_N8gMsmyB2gsP_uDrCOBMSXDud8BFE130_assertion description "[Rare putative mutations in the PCP genes VANGL2, SCRIB, DACT1, and CELSR1 cumulatively contributed to over 20% of cases with craniorachischisis, a rare defect; no contributing variants were found for PRICKLE1 or PTK7.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1016690.RAy06Vc3XjCpyBY_N8gMsmyB2gsP_uDrCOBMSXDud8BFE130_provenance.