Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP485797.RAdzXiBsNmOSQTJvdBojGq4MXNbF5F0ermPNw3zqtm-FI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP485797.RAdzXiBsNmOSQTJvdBojGq4MXNbF5F0ermPNw3zqtm-FI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP485797.RAdzXiBsNmOSQTJvdBojGq4MXNbF5F0ermPNw3zqtm-FI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP485797.RAdzXiBsNmOSQTJvdBojGq4MXNbF5F0ermPNw3zqtm-FI130_provenance.
- NP485797.RAdzXiBsNmOSQTJvdBojGq4MXNbF5F0ermPNw3zqtm-FI130_assertion wasGeneratedBy ECO_0000203 NP485797.RAdzXiBsNmOSQTJvdBojGq4MXNbF5F0ermPNw3zqtm-FI130_provenance.
- NP485797.RAdzXiBsNmOSQTJvdBojGq4MXNbF5F0ermPNw3zqtm-FI130_assertion wasDerivedFrom befree-20140225 NP485797.RAdzXiBsNmOSQTJvdBojGq4MXNbF5F0ermPNw3zqtm-FI130_provenance.
- NP485797.RAdzXiBsNmOSQTJvdBojGq4MXNbF5F0ermPNw3zqtm-FI130_assertion SIO_000772 11558900 NP485797.RAdzXiBsNmOSQTJvdBojGq4MXNbF5F0ermPNw3zqtm-FI130_provenance.
- NP485797.RAdzXiBsNmOSQTJvdBojGq4MXNbF5F0ermPNw3zqtm-FI130_assertion evidence source_evidence_literature NP485797.RAdzXiBsNmOSQTJvdBojGq4MXNbF5F0ermPNw3zqtm-FI130_provenance.
- NP485797.RAdzXiBsNmOSQTJvdBojGq4MXNbF5F0ermPNw3zqtm-FI130_assertion description "[Mutation analysis of the PDS gene and the EYA1 gene, which are reported to be responsible for hearing loss associated with ear anomalies, was performed in 24 deaf patients with various middle and inner ear anomalies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485797.RAdzXiBsNmOSQTJvdBojGq4MXNbF5F0ermPNw3zqtm-FI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP485797.RAdzXiBsNmOSQTJvdBojGq4MXNbF5F0ermPNw3zqtm-FI130_provenance.