Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP509250.RAIqoi3Dh5a6fjkFBAkLSLN5XlThiOp0qHkflQqpD6JKU130_assertion> ?p ?o ?g. }
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- NP509250.RAIqoi3Dh5a6fjkFBAkLSLN5XlThiOp0qHkflQqpD6JKU130_assertion type Assertion NP509250.RAIqoi3Dh5a6fjkFBAkLSLN5XlThiOp0qHkflQqpD6JKU130_head.
- 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.
- NP509250.RAIqoi3Dh5a6fjkFBAkLSLN5XlThiOp0qHkflQqpD6JKU130_assertion evidence source_evidence_literature NP509250.RAIqoi3Dh5a6fjkFBAkLSLN5XlThiOp0qHkflQqpD6JKU130_provenance.
- NP509250.RAIqoi3Dh5a6fjkFBAkLSLN5XlThiOp0qHkflQqpD6JKU130_assertion SIO_000772 1610568 NP509250.RAIqoi3Dh5a6fjkFBAkLSLN5XlThiOp0qHkflQqpD6JKU130_provenance.
- NP509250.RAIqoi3Dh5a6fjkFBAkLSLN5XlThiOp0qHkflQqpD6JKU130_assertion wasDerivedFrom befree-2016 NP509250.RAIqoi3Dh5a6fjkFBAkLSLN5XlThiOp0qHkflQqpD6JKU130_provenance.
- NP509250.RAIqoi3Dh5a6fjkFBAkLSLN5XlThiOp0qHkflQqpD6JKU130_assertion wasGeneratedBy ECO_0000203 NP509250.RAIqoi3Dh5a6fjkFBAkLSLN5XlThiOp0qHkflQqpD6JKU130_provenance.