Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP231373.RA0XdLrdSGkzd7D_77d0RuEWI9g8EvEXZF8nl-ABu43jM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP231373.RA0XdLrdSGkzd7D_77d0RuEWI9g8EvEXZF8nl-ABu43jM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP231373.RA0XdLrdSGkzd7D_77d0RuEWI9g8EvEXZF8nl-ABu43jM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP231373.RA0XdLrdSGkzd7D_77d0RuEWI9g8EvEXZF8nl-ABu43jM130_provenance.
- NP231373.RA0XdLrdSGkzd7D_77d0RuEWI9g8EvEXZF8nl-ABu43jM130_assertion description "[In humans, we identified recessive loss-of-function DYX1C1 mutations in 12 individuals with PCD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP231373.RA0XdLrdSGkzd7D_77d0RuEWI9g8EvEXZF8nl-ABu43jM130_provenance.
- NP231373.RA0XdLrdSGkzd7D_77d0RuEWI9g8EvEXZF8nl-ABu43jM130_assertion evidence source_evidence_literature NP231373.RA0XdLrdSGkzd7D_77d0RuEWI9g8EvEXZF8nl-ABu43jM130_provenance.
- NP231373.RA0XdLrdSGkzd7D_77d0RuEWI9g8EvEXZF8nl-ABu43jM130_assertion SIO_000772 23872636 NP231373.RA0XdLrdSGkzd7D_77d0RuEWI9g8EvEXZF8nl-ABu43jM130_provenance.
- NP231373.RA0XdLrdSGkzd7D_77d0RuEWI9g8EvEXZF8nl-ABu43jM130_assertion wasDerivedFrom befree-20140225 NP231373.RA0XdLrdSGkzd7D_77d0RuEWI9g8EvEXZF8nl-ABu43jM130_provenance.
- NP231373.RA0XdLrdSGkzd7D_77d0RuEWI9g8EvEXZF8nl-ABu43jM130_assertion wasGeneratedBy ECO_0000203 NP231373.RA0XdLrdSGkzd7D_77d0RuEWI9g8EvEXZF8nl-ABu43jM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP231373.RA0XdLrdSGkzd7D_77d0RuEWI9g8EvEXZF8nl-ABu43jM130_provenance.