Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP668581.RAMxGKN8o6d4cmhNoKRV3s8sXZb2WbGIcPcTqiUStMMVw130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP668581.RAMxGKN8o6d4cmhNoKRV3s8sXZb2WbGIcPcTqiUStMMVw130_assertion type Assertion NP668581.RAMxGKN8o6d4cmhNoKRV3s8sXZb2WbGIcPcTqiUStMMVw130_head.
- NP668581.RAMxGKN8o6d4cmhNoKRV3s8sXZb2WbGIcPcTqiUStMMVw130_assertion description "[The purpose of this study was to determine the prevalence of mutations in the peripherin/RDS gene in Spanish patients with different types of autosomal dominant macular dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668581.RAMxGKN8o6d4cmhNoKRV3s8sXZb2WbGIcPcTqiUStMMVw130_provenance.
- NP668581.RAMxGKN8o6d4cmhNoKRV3s8sXZb2WbGIcPcTqiUStMMVw130_assertion evidence source_evidence_literature NP668581.RAMxGKN8o6d4cmhNoKRV3s8sXZb2WbGIcPcTqiUStMMVw130_provenance.
- NP668581.RAMxGKN8o6d4cmhNoKRV3s8sXZb2WbGIcPcTqiUStMMVw130_assertion SIO_000772 17653047 NP668581.RAMxGKN8o6d4cmhNoKRV3s8sXZb2WbGIcPcTqiUStMMVw130_provenance.
- NP668581.RAMxGKN8o6d4cmhNoKRV3s8sXZb2WbGIcPcTqiUStMMVw130_assertion wasDerivedFrom befree-20150227 NP668581.RAMxGKN8o6d4cmhNoKRV3s8sXZb2WbGIcPcTqiUStMMVw130_provenance.
- NP668581.RAMxGKN8o6d4cmhNoKRV3s8sXZb2WbGIcPcTqiUStMMVw130_assertion wasGeneratedBy ECO_0000203 NP668581.RAMxGKN8o6d4cmhNoKRV3s8sXZb2WbGIcPcTqiUStMMVw130_provenance.