Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP384929.RA3mVGLuWwMVmzzMgeeRG77zDFpMF5cnwfk1POIaqdEJo130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP384929.RA3mVGLuWwMVmzzMgeeRG77zDFpMF5cnwfk1POIaqdEJo130_assertion type Assertion NP384929.RA3mVGLuWwMVmzzMgeeRG77zDFpMF5cnwfk1POIaqdEJo130_head.
- NP384929.RA3mVGLuWwMVmzzMgeeRG77zDFpMF5cnwfk1POIaqdEJo130_assertion description "[Mutations in DNAH11 are a common cause of PCD in patients without ciliary ultrastructural defects; thus, genetic analysis can be used to ascertain the diagnosis of PCD in this challenging group of patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP384929.RA3mVGLuWwMVmzzMgeeRG77zDFpMF5cnwfk1POIaqdEJo130_provenance.
- NP384929.RA3mVGLuWwMVmzzMgeeRG77zDFpMF5cnwfk1POIaqdEJo130_assertion evidence source_evidence_literature NP384929.RA3mVGLuWwMVmzzMgeeRG77zDFpMF5cnwfk1POIaqdEJo130_provenance.
- NP384929.RA3mVGLuWwMVmzzMgeeRG77zDFpMF5cnwfk1POIaqdEJo130_assertion SIO_000772 22184204 NP384929.RA3mVGLuWwMVmzzMgeeRG77zDFpMF5cnwfk1POIaqdEJo130_provenance.
- NP384929.RA3mVGLuWwMVmzzMgeeRG77zDFpMF5cnwfk1POIaqdEJo130_assertion wasDerivedFrom befree-20140225 NP384929.RA3mVGLuWwMVmzzMgeeRG77zDFpMF5cnwfk1POIaqdEJo130_provenance.
- NP384929.RA3mVGLuWwMVmzzMgeeRG77zDFpMF5cnwfk1POIaqdEJo130_assertion wasGeneratedBy ECO_0000203 NP384929.RA3mVGLuWwMVmzzMgeeRG77zDFpMF5cnwfk1POIaqdEJo130_provenance.