Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP826910.RAC7z4eWMIKhR1XuVOSc3w6TIiP-N125nqmrbCYfFVPMg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP826910.RAC7z4eWMIKhR1XuVOSc3w6TIiP-N125nqmrbCYfFVPMg130_assertion type Assertion NP826910.RAC7z4eWMIKhR1XuVOSc3w6TIiP-N125nqmrbCYfFVPMg130_head.
- NP826910.RAC7z4eWMIKhR1XuVOSc3w6TIiP-N125nqmrbCYfFVPMg130_assertion wasGeneratedBy ECO_0000203 NP826910.RAC7z4eWMIKhR1XuVOSc3w6TIiP-N125nqmrbCYfFVPMg130_provenance.
- NP826910.RAC7z4eWMIKhR1XuVOSc3w6TIiP-N125nqmrbCYfFVPMg130_assertion wasDerivedFrom befree-2016 NP826910.RAC7z4eWMIKhR1XuVOSc3w6TIiP-N125nqmrbCYfFVPMg130_provenance.
- NP826910.RAC7z4eWMIKhR1XuVOSc3w6TIiP-N125nqmrbCYfFVPMg130_assertion SIO_000772 20642360 NP826910.RAC7z4eWMIKhR1XuVOSc3w6TIiP-N125nqmrbCYfFVPMg130_provenance.
- NP826910.RAC7z4eWMIKhR1XuVOSc3w6TIiP-N125nqmrbCYfFVPMg130_assertion evidence source_evidence_literature NP826910.RAC7z4eWMIKhR1XuVOSc3w6TIiP-N125nqmrbCYfFVPMg130_provenance.
- NP826910.RAC7z4eWMIKhR1XuVOSc3w6TIiP-N125nqmrbCYfFVPMg130_assertion description "[We screened the MYO15A gene for mutations in 104 unrelated multiplex and consanguineous Turkish families with autosomal recessive nonsyndromic sensorineural hearing loss using autozygosity mapping.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP826910.RAC7z4eWMIKhR1XuVOSc3w6TIiP-N125nqmrbCYfFVPMg130_provenance.