Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP562139.RAjC3Rt7fpJqtNF04y-Y6nTqr2d2DOBMfzNcRkAtL2JHE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP562139.RAjC3Rt7fpJqtNF04y-Y6nTqr2d2DOBMfzNcRkAtL2JHE130_assertion type Assertion NP562139.RAjC3Rt7fpJqtNF04y-Y6nTqr2d2DOBMfzNcRkAtL2JHE130_head.
- NP562139.RAjC3Rt7fpJqtNF04y-Y6nTqr2d2DOBMfzNcRkAtL2JHE130_assertion description "[Genes causing nonsyndromic autosomal recessive deafness (DFNB12) and deafness associated with retinitis pigmentosa and vestibular dysfunction (USH1D) were previously mapped to overlapping regions of chromosome 10q21-q22.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP562139.RAjC3Rt7fpJqtNF04y-Y6nTqr2d2DOBMfzNcRkAtL2JHE130_provenance.
- NP562139.RAjC3Rt7fpJqtNF04y-Y6nTqr2d2DOBMfzNcRkAtL2JHE130_assertion evidence source_evidence_literature NP562139.RAjC3Rt7fpJqtNF04y-Y6nTqr2d2DOBMfzNcRkAtL2JHE130_provenance.
- NP562139.RAjC3Rt7fpJqtNF04y-Y6nTqr2d2DOBMfzNcRkAtL2JHE130_assertion SIO_000772 11090341 NP562139.RAjC3Rt7fpJqtNF04y-Y6nTqr2d2DOBMfzNcRkAtL2JHE130_provenance.
- NP562139.RAjC3Rt7fpJqtNF04y-Y6nTqr2d2DOBMfzNcRkAtL2JHE130_assertion wasDerivedFrom befree-20140225 NP562139.RAjC3Rt7fpJqtNF04y-Y6nTqr2d2DOBMfzNcRkAtL2JHE130_provenance.
- NP562139.RAjC3Rt7fpJqtNF04y-Y6nTqr2d2DOBMfzNcRkAtL2JHE130_assertion wasGeneratedBy ECO_0000203 NP562139.RAjC3Rt7fpJqtNF04y-Y6nTqr2d2DOBMfzNcRkAtL2JHE130_provenance.