Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP384929.RA3mVGLuWwMVmzzMgeeRG77zDFpMF5cnwfk1POIaqdEJo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP384929.RA3mVGLuWwMVmzzMgeeRG77zDFpMF5cnwfk1POIaqdEJo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP384929.RA3mVGLuWwMVmzzMgeeRG77zDFpMF5cnwfk1POIaqdEJo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP384929.RA3mVGLuWwMVmzzMgeeRG77zDFpMF5cnwfk1POIaqdEJo130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP384929.RA3mVGLuWwMVmzzMgeeRG77zDFpMF5cnwfk1POIaqdEJo130_provenance.