Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP913807.RAeJzC9VTjM8_ug_Tdw8OBA1ctYQDgiRHk5OHjXpua-Cs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP913807.RAeJzC9VTjM8_ug_Tdw8OBA1ctYQDgiRHk5OHjXpua-Cs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP913807.RAeJzC9VTjM8_ug_Tdw8OBA1ctYQDgiRHk5OHjXpua-Cs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP913807.RAeJzC9VTjM8_ug_Tdw8OBA1ctYQDgiRHk5OHjXpua-Cs130_provenance.
- NP913807.RAeJzC9VTjM8_ug_Tdw8OBA1ctYQDgiRHk5OHjXpua-Cs130_assertion description "[IL17RD mutations were found only in KS individuals and were strongly linked to hearing loss (6/8 individuals).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP913807.RAeJzC9VTjM8_ug_Tdw8OBA1ctYQDgiRHk5OHjXpua-Cs130_provenance.
- NP913807.RAeJzC9VTjM8_ug_Tdw8OBA1ctYQDgiRHk5OHjXpua-Cs130_assertion evidence source_evidence_literature NP913807.RAeJzC9VTjM8_ug_Tdw8OBA1ctYQDgiRHk5OHjXpua-Cs130_provenance.
- NP913807.RAeJzC9VTjM8_ug_Tdw8OBA1ctYQDgiRHk5OHjXpua-Cs130_assertion SIO_000772 23643382 NP913807.RAeJzC9VTjM8_ug_Tdw8OBA1ctYQDgiRHk5OHjXpua-Cs130_provenance.
- NP913807.RAeJzC9VTjM8_ug_Tdw8OBA1ctYQDgiRHk5OHjXpua-Cs130_assertion wasDerivedFrom befree-20150227 NP913807.RAeJzC9VTjM8_ug_Tdw8OBA1ctYQDgiRHk5OHjXpua-Cs130_provenance.
- NP913807.RAeJzC9VTjM8_ug_Tdw8OBA1ctYQDgiRHk5OHjXpua-Cs130_assertion wasGeneratedBy ECO_0000203 NP913807.RAeJzC9VTjM8_ug_Tdw8OBA1ctYQDgiRHk5OHjXpua-Cs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP913807.RAeJzC9VTjM8_ug_Tdw8OBA1ctYQDgiRHk5OHjXpua-Cs130_provenance.