Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP811392.RAb-gnmzrXvmSGEf5KvnwW9bpUvAm9Blzcv0h6x2roXfA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP811392.RAb-gnmzrXvmSGEf5KvnwW9bpUvAm9Blzcv0h6x2roXfA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP811392.RAb-gnmzrXvmSGEf5KvnwW9bpUvAm9Blzcv0h6x2roXfA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP811392.RAb-gnmzrXvmSGEf5KvnwW9bpUvAm9Blzcv0h6x2roXfA130_provenance.
- NP811392.RAb-gnmzrXvmSGEf5KvnwW9bpUvAm9Blzcv0h6x2roXfA130_assertion description "[We found a different distribution of allelic frequency of AAT repeats in the CNR1 gene in healthy controls and IBS patients, and a significant association between the CNR1 >10/>10 genotype and IBS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP811392.RAb-gnmzrXvmSGEf5KvnwW9bpUvAm9Blzcv0h6x2roXfA130_provenance.
- NP811392.RAb-gnmzrXvmSGEf5KvnwW9bpUvAm9Blzcv0h6x2roXfA130_assertion evidence source_evidence_literature NP811392.RAb-gnmzrXvmSGEf5KvnwW9bpUvAm9Blzcv0h6x2roXfA130_provenance.
- NP811392.RAb-gnmzrXvmSGEf5KvnwW9bpUvAm9Blzcv0h6x2roXfA130_assertion SIO_000772 20505532 NP811392.RAb-gnmzrXvmSGEf5KvnwW9bpUvAm9Blzcv0h6x2roXfA130_provenance.
- NP811392.RAb-gnmzrXvmSGEf5KvnwW9bpUvAm9Blzcv0h6x2roXfA130_assertion wasDerivedFrom befree-20140225 NP811392.RAb-gnmzrXvmSGEf5KvnwW9bpUvAm9Blzcv0h6x2roXfA130_provenance.
- NP811392.RAb-gnmzrXvmSGEf5KvnwW9bpUvAm9Blzcv0h6x2roXfA130_assertion wasGeneratedBy ECO_0000203 NP811392.RAb-gnmzrXvmSGEf5KvnwW9bpUvAm9Blzcv0h6x2roXfA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP811392.RAb-gnmzrXvmSGEf5KvnwW9bpUvAm9Blzcv0h6x2roXfA130_provenance.