Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1205350.RAQlJGZw_G8CIm7fjt_xAGhk-B9eqjal6J143tD2ZMKbY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1205350.RAQlJGZw_G8CIm7fjt_xAGhk-B9eqjal6J143tD2ZMKbY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1205350.RAQlJGZw_G8CIm7fjt_xAGhk-B9eqjal6J143tD2ZMKbY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1205350.RAQlJGZw_G8CIm7fjt_xAGhk-B9eqjal6J143tD2ZMKbY130_provenance.
- befree-2016 importedOn "2016-02-19" NP1205350.RAQlJGZw_G8CIm7fjt_xAGhk-B9eqjal6J143tD2ZMKbY130_provenance.
- NP1205350.RAQlJGZw_G8CIm7fjt_xAGhk-B9eqjal6J143tD2ZMKbY130_assertion wasGeneratedBy ECO_0000203 NP1205350.RAQlJGZw_G8CIm7fjt_xAGhk-B9eqjal6J143tD2ZMKbY130_provenance.
- NP1205350.RAQlJGZw_G8CIm7fjt_xAGhk-B9eqjal6J143tD2ZMKbY130_assertion wasDerivedFrom befree-2016 NP1205350.RAQlJGZw_G8CIm7fjt_xAGhk-B9eqjal6J143tD2ZMKbY130_provenance.
- NP1205350.RAQlJGZw_G8CIm7fjt_xAGhk-B9eqjal6J143tD2ZMKbY130_assertion SIO_000772 25066065 NP1205350.RAQlJGZw_G8CIm7fjt_xAGhk-B9eqjal6J143tD2ZMKbY130_provenance.
- NP1205350.RAQlJGZw_G8CIm7fjt_xAGhk-B9eqjal6J143tD2ZMKbY130_assertion evidence source_evidence_literature NP1205350.RAQlJGZw_G8CIm7fjt_xAGhk-B9eqjal6J143tD2ZMKbY130_provenance.
- NP1205350.RAQlJGZw_G8CIm7fjt_xAGhk-B9eqjal6J143tD2ZMKbY130_assertion description "[PCD can be caused by hemizygous DNAH5 mutation in combination with a 5p segmental deletion attributable to CdCS on the opposite chromosome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1205350.RAQlJGZw_G8CIm7fjt_xAGhk-B9eqjal6J143tD2ZMKbY130_provenance.