Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP913807.RAeJzC9VTjM8_ug_Tdw8OBA1ctYQDgiRHk5OHjXpua-Cs130_assertion> ?p ?o ?g. }
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- NP913807.RAeJzC9VTjM8_ug_Tdw8OBA1ctYQDgiRHk5OHjXpua-Cs130_assertion type Assertion NP913807.RAeJzC9VTjM8_ug_Tdw8OBA1ctYQDgiRHk5OHjXpua-Cs130_head.
- 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.