Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1042462.RAWjnRJa3L_I3UssUglwCCw-KhmG12jwCEy2umBB0ntSM130_assertion> ?p ?o ?g. }
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- NP1042462.RAWjnRJa3L_I3UssUglwCCw-KhmG12jwCEy2umBB0ntSM130_assertion type Assertion NP1042462.RAWjnRJa3L_I3UssUglwCCw-KhmG12jwCEy2umBB0ntSM130_head.
- NP1042462.RAWjnRJa3L_I3UssUglwCCw-KhmG12jwCEy2umBB0ntSM130_assertion description "[Two novel disease-causing mutations in the CLRN1 gene in patients with Usher syndrome type 3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1042462.RAWjnRJa3L_I3UssUglwCCw-KhmG12jwCEy2umBB0ntSM130_provenance.
- NP1042462.RAWjnRJa3L_I3UssUglwCCw-KhmG12jwCEy2umBB0ntSM130_assertion evidence source_evidence_literature NP1042462.RAWjnRJa3L_I3UssUglwCCw-KhmG12jwCEy2umBB0ntSM130_provenance.
- NP1042462.RAWjnRJa3L_I3UssUglwCCw-KhmG12jwCEy2umBB0ntSM130_assertion SIO_000772 23304067 NP1042462.RAWjnRJa3L_I3UssUglwCCw-KhmG12jwCEy2umBB0ntSM130_provenance.
- NP1042462.RAWjnRJa3L_I3UssUglwCCw-KhmG12jwCEy2umBB0ntSM130_assertion wasDerivedFrom befree-2016 NP1042462.RAWjnRJa3L_I3UssUglwCCw-KhmG12jwCEy2umBB0ntSM130_provenance.
- NP1042462.RAWjnRJa3L_I3UssUglwCCw-KhmG12jwCEy2umBB0ntSM130_assertion wasGeneratedBy ECO_0000203 NP1042462.RAWjnRJa3L_I3UssUglwCCw-KhmG12jwCEy2umBB0ntSM130_provenance.