Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP3967.RAE21H9mgbxRJ6qbjBXVHKlqoQJjvnRvaCI-6jUkVV2Y4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP3967.RAE21H9mgbxRJ6qbjBXVHKlqoQJjvnRvaCI-6jUkVV2Y4130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP3967.RAE21H9mgbxRJ6qbjBXVHKlqoQJjvnRvaCI-6jUkVV2Y4130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP3967.RAE21H9mgbxRJ6qbjBXVHKlqoQJjvnRvaCI-6jUkVV2Y4130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP3967.RAE21H9mgbxRJ6qbjBXVHKlqoQJjvnRvaCI-6jUkVV2Y4130_provenance.
- NP3967.RAE21H9mgbxRJ6qbjBXVHKlqoQJjvnRvaCI-6jUkVV2Y4130_assertion wasGeneratedBy ECO_0000218 NP3967.RAE21H9mgbxRJ6qbjBXVHKlqoQJjvnRvaCI-6jUkVV2Y4130_provenance.
- NP3967.RAE21H9mgbxRJ6qbjBXVHKlqoQJjvnRvaCI-6jUkVV2Y4130_assertion wasDerivedFrom uniprot-20150221 NP3967.RAE21H9mgbxRJ6qbjBXVHKlqoQJjvnRvaCI-6jUkVV2Y4130_provenance.
- NP3967.RAE21H9mgbxRJ6qbjBXVHKlqoQJjvnRvaCI-6jUkVV2Y4130_assertion SIO_000772 14506070 NP3967.RAE21H9mgbxRJ6qbjBXVHKlqoQJjvnRvaCI-6jUkVV2Y4130_provenance.
- NP3967.RAE21H9mgbxRJ6qbjBXVHKlqoQJjvnRvaCI-6jUkVV2Y4130_assertion evidence source_evidence_curated NP3967.RAE21H9mgbxRJ6qbjBXVHKlqoQJjvnRvaCI-6jUkVV2Y4130_provenance.
- NP3967.RAE21H9mgbxRJ6qbjBXVHKlqoQJjvnRvaCI-6jUkVV2Y4130_assertion description "[Cerebellar ataxia with oculomotor apraxia type 1: clinical and genetic studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3967.RAE21H9mgbxRJ6qbjBXVHKlqoQJjvnRvaCI-6jUkVV2Y4130_provenance.