Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP697610.RAPOFBsFiRxHbfgqSZVToSwenvxO0a3IbkX9Sy2p09dQA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP697610.RAPOFBsFiRxHbfgqSZVToSwenvxO0a3IbkX9Sy2p09dQA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP697610.RAPOFBsFiRxHbfgqSZVToSwenvxO0a3IbkX9Sy2p09dQA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP697610.RAPOFBsFiRxHbfgqSZVToSwenvxO0a3IbkX9Sy2p09dQA130_provenance.
- NP697610.RAPOFBsFiRxHbfgqSZVToSwenvxO0a3IbkX9Sy2p09dQA130_assertion description "[82 exons and intron/exon junctions in DNAH11 were sequenced in 163 unrelated patients with a clinical phenotype of PCD, including those with normal ciliary ultrastructure (n=58), defects in outer and/or inner dynein arms (n=76), radial spoke/central pair defects (n=6), and 23 without definitive ultrastructural results, but who had situs inversus (n=17), or bronchiectasis and/or low nasal nitric oxide (n=6).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP697610.RAPOFBsFiRxHbfgqSZVToSwenvxO0a3IbkX9Sy2p09dQA130_provenance.
- NP697610.RAPOFBsFiRxHbfgqSZVToSwenvxO0a3IbkX9Sy2p09dQA130_assertion evidence source_evidence_literature NP697610.RAPOFBsFiRxHbfgqSZVToSwenvxO0a3IbkX9Sy2p09dQA130_provenance.
- NP697610.RAPOFBsFiRxHbfgqSZVToSwenvxO0a3IbkX9Sy2p09dQA130_assertion SIO_000772 22184204 NP697610.RAPOFBsFiRxHbfgqSZVToSwenvxO0a3IbkX9Sy2p09dQA130_provenance.
- NP697610.RAPOFBsFiRxHbfgqSZVToSwenvxO0a3IbkX9Sy2p09dQA130_assertion wasDerivedFrom befree-20140225 NP697610.RAPOFBsFiRxHbfgqSZVToSwenvxO0a3IbkX9Sy2p09dQA130_provenance.
- NP697610.RAPOFBsFiRxHbfgqSZVToSwenvxO0a3IbkX9Sy2p09dQA130_assertion wasGeneratedBy ECO_0000203 NP697610.RAPOFBsFiRxHbfgqSZVToSwenvxO0a3IbkX9Sy2p09dQA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP697610.RAPOFBsFiRxHbfgqSZVToSwenvxO0a3IbkX9Sy2p09dQA130_provenance.