Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP512334.RA773KN6ZUJF8Tm17oWP_kmokWdh9Cyw2Ic5o87R3IDdU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP512334.RA773KN6ZUJF8Tm17oWP_kmokWdh9Cyw2Ic5o87R3IDdU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP512334.RA773KN6ZUJF8Tm17oWP_kmokWdh9Cyw2Ic5o87R3IDdU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP512334.RA773KN6ZUJF8Tm17oWP_kmokWdh9Cyw2Ic5o87R3IDdU130_provenance.
- NP512334.RA773KN6ZUJF8Tm17oWP_kmokWdh9Cyw2Ic5o87R3IDdU130_assertion description "[To test further for mutant DNAH11 as a cause of PCD, DNAH11 was sequenced in patients with a PCD clinical phenotype, but no known genetic aetiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP512334.RA773KN6ZUJF8Tm17oWP_kmokWdh9Cyw2Ic5o87R3IDdU130_provenance.
- NP512334.RA773KN6ZUJF8Tm17oWP_kmokWdh9Cyw2Ic5o87R3IDdU130_assertion evidence source_evidence_literature NP512334.RA773KN6ZUJF8Tm17oWP_kmokWdh9Cyw2Ic5o87R3IDdU130_provenance.
- NP512334.RA773KN6ZUJF8Tm17oWP_kmokWdh9Cyw2Ic5o87R3IDdU130_assertion SIO_000772 22184204 NP512334.RA773KN6ZUJF8Tm17oWP_kmokWdh9Cyw2Ic5o87R3IDdU130_provenance.
- NP512334.RA773KN6ZUJF8Tm17oWP_kmokWdh9Cyw2Ic5o87R3IDdU130_assertion wasDerivedFrom befree-20140225 NP512334.RA773KN6ZUJF8Tm17oWP_kmokWdh9Cyw2Ic5o87R3IDdU130_provenance.
- NP512334.RA773KN6ZUJF8Tm17oWP_kmokWdh9Cyw2Ic5o87R3IDdU130_assertion wasGeneratedBy ECO_0000203 NP512334.RA773KN6ZUJF8Tm17oWP_kmokWdh9Cyw2Ic5o87R3IDdU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP512334.RA773KN6ZUJF8Tm17oWP_kmokWdh9Cyw2Ic5o87R3IDdU130_provenance.