Matches in Nanopublications for { ?s ?p "[The association of mutations in RDS with retinitis pigmentosa indicates that ROM1 is a strong candidate gene for human retinopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 8 of
8
with 100 items per page.
- NP298877.RAhm6g8Xql13fMWeh4ozCg2clKuwYDMfKfghcYidE_91c130_assertion description "[The association of mutations in RDS with retinitis pigmentosa indicates that ROM1 is a strong candidate gene for human retinopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP298877.RAhm6g8Xql13fMWeh4ozCg2clKuwYDMfKfghcYidE_91c130_provenance.
- NP492714.RA6__-yTxGsUd1h0O3au7M0_UoLMoz-RPM6L5Krlk1HF0130_assertion description "[The association of mutations in RDS with retinitis pigmentosa indicates that ROM1 is a strong candidate gene for human retinopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP492714.RA6__-yTxGsUd1h0O3au7M0_UoLMoz-RPM6L5Krlk1HF0130_provenance.
- NP855464.RAyRRpmrBeMv1ZPNZEZybu8A3zrIXFjzuYKQihRlm4QQI130_assertion description "[The association of mutations in RDS with retinitis pigmentosa indicates that ROM1 is a strong candidate gene for human retinopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP855464.RAyRRpmrBeMv1ZPNZEZybu8A3zrIXFjzuYKQihRlm4QQI130_provenance.
- NP584923.RAG5_ppWWcXFIqzerPKvJBdCEh8WmKjgdZvdbch9FHsmM130_assertion description "[The association of mutations in RDS with retinitis pigmentosa indicates that ROM1 is a strong candidate gene for human retinopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP584923.RAG5_ppWWcXFIqzerPKvJBdCEh8WmKjgdZvdbch9FHsmM130_provenance.
- assertion description "[The association of mutations in RDS with retinitis pigmentosa indicates that ROM1 is a strong candidate gene for human retinopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP824790.RAGKFyJhQ91fsZMYvr13vfWwkzkC7rOIWkx_k03B1Ivow130_assertion description "[The association of mutations in RDS with retinitis pigmentosa indicates that ROM1 is a strong candidate gene for human retinopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP824790.RAGKFyJhQ91fsZMYvr13vfWwkzkC7rOIWkx_k03B1Ivow130_provenance.
- NP509250.RAIqoi3Dh5a6fjkFBAkLSLN5XlThiOp0qHkflQqpD6JKU130_assertion description "[The association of mutations in RDS with retinitis pigmentosa indicates that ROM1 is a strong candidate gene for human retinopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP509250.RAIqoi3Dh5a6fjkFBAkLSLN5XlThiOp0qHkflQqpD6JKU130_provenance.
- NP674084.RA80OtWhh5TToEtOYCrhjOtW8WRC-8ldKLOp0YSZqgDqI130_assertion description "[The association of mutations in RDS with retinitis pigmentosa indicates that ROM1 is a strong candidate gene for human retinopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674084.RA80OtWhh5TToEtOYCrhjOtW8WRC-8ldKLOp0YSZqgDqI130_provenance.