Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP251310.RAH-sPS0oe2MwvX1ye65JeIhchXKtfGFNywC43J2IIvdA130_assertion> ?p ?o ?g. }
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- NP251310.RAH-sPS0oe2MwvX1ye65JeIhchXKtfGFNywC43J2IIvdA130_assertion type Assertion NP251310.RAH-sPS0oe2MwvX1ye65JeIhchXKtfGFNywC43J2IIvdA130_head.
- NP251310.RAH-sPS0oe2MwvX1ye65JeIhchXKtfGFNywC43J2IIvdA130_assertion description "[Sanger sequencing of 67 additional individuals with PCD with ODA defects from 58 families revealed CCDC114 mutations in 4 individuals in 3 families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP251310.RAH-sPS0oe2MwvX1ye65JeIhchXKtfGFNywC43J2IIvdA130_provenance.
- NP251310.RAH-sPS0oe2MwvX1ye65JeIhchXKtfGFNywC43J2IIvdA130_assertion evidence source_evidence_literature NP251310.RAH-sPS0oe2MwvX1ye65JeIhchXKtfGFNywC43J2IIvdA130_provenance.
- NP251310.RAH-sPS0oe2MwvX1ye65JeIhchXKtfGFNywC43J2IIvdA130_assertion SIO_000772 23261302 NP251310.RAH-sPS0oe2MwvX1ye65JeIhchXKtfGFNywC43J2IIvdA130_provenance.
- NP251310.RAH-sPS0oe2MwvX1ye65JeIhchXKtfGFNywC43J2IIvdA130_assertion wasDerivedFrom befree-20140225 NP251310.RAH-sPS0oe2MwvX1ye65JeIhchXKtfGFNywC43J2IIvdA130_provenance.
- NP251310.RAH-sPS0oe2MwvX1ye65JeIhchXKtfGFNywC43J2IIvdA130_assertion wasGeneratedBy ECO_0000203 NP251310.RAH-sPS0oe2MwvX1ye65JeIhchXKtfGFNywC43J2IIvdA130_provenance.