Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP509250.RAIqoi3Dh5a6fjkFBAkLSLN5XlThiOp0qHkflQqpD6JKU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP509250.RAIqoi3Dh5a6fjkFBAkLSLN5XlThiOp0qHkflQqpD6JKU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP509250.RAIqoi3Dh5a6fjkFBAkLSLN5XlThiOp0qHkflQqpD6JKU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP509250.RAIqoi3Dh5a6fjkFBAkLSLN5XlThiOp0qHkflQqpD6JKU130_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.
- 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.
- befree-2016 importedOn "2016-02-19" NP509250.RAIqoi3Dh5a6fjkFBAkLSLN5XlThiOp0qHkflQqpD6JKU130_provenance.