Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP283864.RAtaeUrTJdP8pj1jqmxPoWD7GaQ_yr7Uc3zFRBw7WBpuU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP283864.RAtaeUrTJdP8pj1jqmxPoWD7GaQ_yr7Uc3zFRBw7WBpuU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP283864.RAtaeUrTJdP8pj1jqmxPoWD7GaQ_yr7Uc3zFRBw7WBpuU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP283864.RAtaeUrTJdP8pj1jqmxPoWD7GaQ_yr7Uc3zFRBw7WBpuU130_provenance.
- NP283864.RAtaeUrTJdP8pj1jqmxPoWD7GaQ_yr7Uc3zFRBw7WBpuU130_assertion description "[In conclusion, the NOS3 and Cav1 polymorphisms were significantly associated with the risk of SSNHL and M�ni�re's disease, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP283864.RAtaeUrTJdP8pj1jqmxPoWD7GaQ_yr7Uc3zFRBw7WBpuU130_provenance.
- NP283864.RAtaeUrTJdP8pj1jqmxPoWD7GaQ_yr7Uc3zFRBw7WBpuU130_assertion evidence source_evidence_literature NP283864.RAtaeUrTJdP8pj1jqmxPoWD7GaQ_yr7Uc3zFRBw7WBpuU130_provenance.
- NP283864.RAtaeUrTJdP8pj1jqmxPoWD7GaQ_yr7Uc3zFRBw7WBpuU130_assertion SIO_000772 23560644 NP283864.RAtaeUrTJdP8pj1jqmxPoWD7GaQ_yr7Uc3zFRBw7WBpuU130_provenance.
- NP283864.RAtaeUrTJdP8pj1jqmxPoWD7GaQ_yr7Uc3zFRBw7WBpuU130_assertion wasDerivedFrom befree-20150227 NP283864.RAtaeUrTJdP8pj1jqmxPoWD7GaQ_yr7Uc3zFRBw7WBpuU130_provenance.
- NP283864.RAtaeUrTJdP8pj1jqmxPoWD7GaQ_yr7Uc3zFRBw7WBpuU130_assertion wasGeneratedBy ECO_0000203 NP283864.RAtaeUrTJdP8pj1jqmxPoWD7GaQ_yr7Uc3zFRBw7WBpuU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP283864.RAtaeUrTJdP8pj1jqmxPoWD7GaQ_yr7Uc3zFRBw7WBpuU130_provenance.