Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP221814.RAptH8w_gQtFT5jyjnhL8PcCS5ajPPMjKS2o6BCqeDTOM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP221814.RAptH8w_gQtFT5jyjnhL8PcCS5ajPPMjKS2o6BCqeDTOM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP221814.RAptH8w_gQtFT5jyjnhL8PcCS5ajPPMjKS2o6BCqeDTOM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP221814.RAptH8w_gQtFT5jyjnhL8PcCS5ajPPMjKS2o6BCqeDTOM130_provenance.
- NP221814.RAptH8w_gQtFT5jyjnhL8PcCS5ajPPMjKS2o6BCqeDTOM130_assertion description "[Here, we identify mutations in Gipc3 underlying progressive sensorineural hearing loss (age-related hearing loss 5, ahl5) and audiogenic seizures (juvenile audiogenic monogenic seizure 1, jams1) in mice and autosomal recessive deafness DFNB15 and DFNB95 in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221814.RAptH8w_gQtFT5jyjnhL8PcCS5ajPPMjKS2o6BCqeDTOM130_provenance.
- NP221814.RAptH8w_gQtFT5jyjnhL8PcCS5ajPPMjKS2o6BCqeDTOM130_assertion evidence source_evidence_literature NP221814.RAptH8w_gQtFT5jyjnhL8PcCS5ajPPMjKS2o6BCqeDTOM130_provenance.
- NP221814.RAptH8w_gQtFT5jyjnhL8PcCS5ajPPMjKS2o6BCqeDTOM130_assertion SIO_000772 21326233 NP221814.RAptH8w_gQtFT5jyjnhL8PcCS5ajPPMjKS2o6BCqeDTOM130_provenance.
- NP221814.RAptH8w_gQtFT5jyjnhL8PcCS5ajPPMjKS2o6BCqeDTOM130_assertion wasDerivedFrom befree-20140225 NP221814.RAptH8w_gQtFT5jyjnhL8PcCS5ajPPMjKS2o6BCqeDTOM130_provenance.
- NP221814.RAptH8w_gQtFT5jyjnhL8PcCS5ajPPMjKS2o6BCqeDTOM130_assertion wasGeneratedBy ECO_0000203 NP221814.RAptH8w_gQtFT5jyjnhL8PcCS5ajPPMjKS2o6BCqeDTOM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP221814.RAptH8w_gQtFT5jyjnhL8PcCS5ajPPMjKS2o6BCqeDTOM130_provenance.