Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP584029.RAFUGV_6jcdKoluUpMFW3ZhEHSDylnsmVWhMDlAMSRMnU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP584029.RAFUGV_6jcdKoluUpMFW3ZhEHSDylnsmVWhMDlAMSRMnU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP584029.RAFUGV_6jcdKoluUpMFW3ZhEHSDylnsmVWhMDlAMSRMnU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP584029.RAFUGV_6jcdKoluUpMFW3ZhEHSDylnsmVWhMDlAMSRMnU130_provenance.
- NP584029.RAFUGV_6jcdKoluUpMFW3ZhEHSDylnsmVWhMDlAMSRMnU130_assertion description "[Here, we review the MYO5B gene and all currently known MYO5B mutations and for the first time methodologically categorize these with regard to functional protein domains and recurrence in MYO7A associated with Usher syndrome and other myosins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP584029.RAFUGV_6jcdKoluUpMFW3ZhEHSDylnsmVWhMDlAMSRMnU130_provenance.
- NP584029.RAFUGV_6jcdKoluUpMFW3ZhEHSDylnsmVWhMDlAMSRMnU130_assertion evidence source_evidence_literature NP584029.RAFUGV_6jcdKoluUpMFW3ZhEHSDylnsmVWhMDlAMSRMnU130_provenance.
- NP584029.RAFUGV_6jcdKoluUpMFW3ZhEHSDylnsmVWhMDlAMSRMnU130_assertion SIO_000772 24014347 NP584029.RAFUGV_6jcdKoluUpMFW3ZhEHSDylnsmVWhMDlAMSRMnU130_provenance.
- NP584029.RAFUGV_6jcdKoluUpMFW3ZhEHSDylnsmVWhMDlAMSRMnU130_assertion wasDerivedFrom befree-20150227 NP584029.RAFUGV_6jcdKoluUpMFW3ZhEHSDylnsmVWhMDlAMSRMnU130_provenance.
- NP584029.RAFUGV_6jcdKoluUpMFW3ZhEHSDylnsmVWhMDlAMSRMnU130_assertion wasGeneratedBy ECO_0000203 NP584029.RAFUGV_6jcdKoluUpMFW3ZhEHSDylnsmVWhMDlAMSRMnU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP584029.RAFUGV_6jcdKoluUpMFW3ZhEHSDylnsmVWhMDlAMSRMnU130_provenance.