Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP708852.RAHsVGWIxs2eTVFcc8EB4lXI06FTTfYRFB1N_nns5GrfA130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP708852.RAHsVGWIxs2eTVFcc8EB4lXI06FTTfYRFB1N_nns5GrfA130_assertion type Assertion NP708852.RAHsVGWIxs2eTVFcc8EB4lXI06FTTfYRFB1N_nns5GrfA130_head.
- NP708852.RAHsVGWIxs2eTVFcc8EB4lXI06FTTfYRFB1N_nns5GrfA130_assertion description "[Mutations in SRY, SOX9 and SOX10 have been shown to be responsible for XY sex reversal, campomelic dysplasia and Waardenburg-Hirschsprung disease, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP708852.RAHsVGWIxs2eTVFcc8EB4lXI06FTTfYRFB1N_nns5GrfA130_provenance.
- NP708852.RAHsVGWIxs2eTVFcc8EB4lXI06FTTfYRFB1N_nns5GrfA130_assertion evidence source_evidence_literature NP708852.RAHsVGWIxs2eTVFcc8EB4lXI06FTTfYRFB1N_nns5GrfA130_provenance.
- NP708852.RAHsVGWIxs2eTVFcc8EB4lXI06FTTfYRFB1N_nns5GrfA130_assertion SIO_000772 10798354 NP708852.RAHsVGWIxs2eTVFcc8EB4lXI06FTTfYRFB1N_nns5GrfA130_provenance.
- NP708852.RAHsVGWIxs2eTVFcc8EB4lXI06FTTfYRFB1N_nns5GrfA130_assertion wasDerivedFrom befree-20150227 NP708852.RAHsVGWIxs2eTVFcc8EB4lXI06FTTfYRFB1N_nns5GrfA130_provenance.
- NP708852.RAHsVGWIxs2eTVFcc8EB4lXI06FTTfYRFB1N_nns5GrfA130_assertion wasGeneratedBy ECO_0000203 NP708852.RAHsVGWIxs2eTVFcc8EB4lXI06FTTfYRFB1N_nns5GrfA130_provenance.