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- NP13098.RASf3OFQEJMbkQT5LMwpkjJBaayAFIz_Z_-iJ88gYBnu4130_assertion type Assertion NP13098.RASf3OFQEJMbkQT5LMwpkjJBaayAFIz_Z_-iJ88gYBnu4130_head.
- NP13098.RASf3OFQEJMbkQT5LMwpkjJBaayAFIz_Z_-iJ88gYBnu4130_assertion description "[In humans, we identified recessive loss-of-function DYX1C1 mutations in 12 individuals with PCD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP13098.RASf3OFQEJMbkQT5LMwpkjJBaayAFIz_Z_-iJ88gYBnu4130_provenance.
- NP13098.RASf3OFQEJMbkQT5LMwpkjJBaayAFIz_Z_-iJ88gYBnu4130_assertion evidence source_evidence_curated NP13098.RASf3OFQEJMbkQT5LMwpkjJBaayAFIz_Z_-iJ88gYBnu4130_provenance.
- NP13098.RASf3OFQEJMbkQT5LMwpkjJBaayAFIz_Z_-iJ88gYBnu4130_assertion SIO_000772 23872636 NP13098.RASf3OFQEJMbkQT5LMwpkjJBaayAFIz_Z_-iJ88gYBnu4130_provenance.
- NP13098.RASf3OFQEJMbkQT5LMwpkjJBaayAFIz_Z_-iJ88gYBnu4130_assertion wasDerivedFrom ctd_human-20150221 NP13098.RASf3OFQEJMbkQT5LMwpkjJBaayAFIz_Z_-iJ88gYBnu4130_provenance.
- NP13098.RASf3OFQEJMbkQT5LMwpkjJBaayAFIz_Z_-iJ88gYBnu4130_assertion wasGeneratedBy ECO_0000218 NP13098.RASf3OFQEJMbkQT5LMwpkjJBaayAFIz_Z_-iJ88gYBnu4130_provenance.