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- NP948289.RA_SV1-KvLsltr_AuG8U52edl3QchyHupRIwIGnQukHG0130_assertion type Assertion NP948289.RA_SV1-KvLsltr_AuG8U52edl3QchyHupRIwIGnQukHG0130_head.
- NP948289.RA_SV1-KvLsltr_AuG8U52edl3QchyHupRIwIGnQukHG0130_assertion wasGeneratedBy ECO_0000203 NP948289.RA_SV1-KvLsltr_AuG8U52edl3QchyHupRIwIGnQukHG0130_provenance.
- NP948289.RA_SV1-KvLsltr_AuG8U52edl3QchyHupRIwIGnQukHG0130_assertion wasDerivedFrom befree-20150227 NP948289.RA_SV1-KvLsltr_AuG8U52edl3QchyHupRIwIGnQukHG0130_provenance.
- NP948289.RA_SV1-KvLsltr_AuG8U52edl3QchyHupRIwIGnQukHG0130_assertion SIO_000772 23024041 NP948289.RA_SV1-KvLsltr_AuG8U52edl3QchyHupRIwIGnQukHG0130_provenance.
- NP948289.RA_SV1-KvLsltr_AuG8U52edl3QchyHupRIwIGnQukHG0130_assertion evidence source_evidence_literature NP948289.RA_SV1-KvLsltr_AuG8U52edl3QchyHupRIwIGnQukHG0130_provenance.
- NP948289.RA_SV1-KvLsltr_AuG8U52edl3QchyHupRIwIGnQukHG0130_assertion description "[PCP rare putative mutations had a weaker role in myelomeningocele (SB), being found in approximately 6% of cases and cumulated across CELSR1, FUZ, FZD6, PRICKLE1, VANGL1, and VANGL2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP948289.RA_SV1-KvLsltr_AuG8U52edl3QchyHupRIwIGnQukHG0130_provenance.