Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP115066.RANOVZTCm0vFdF3QsZW6rnOUEaiRUX6nCtA1v7abud1-4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP115066.RANOVZTCm0vFdF3QsZW6rnOUEaiRUX6nCtA1v7abud1-4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP115066.RANOVZTCm0vFdF3QsZW6rnOUEaiRUX6nCtA1v7abud1-4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP115066.RANOVZTCm0vFdF3QsZW6rnOUEaiRUX6nCtA1v7abud1-4130_provenance.
- NP115066.RANOVZTCm0vFdF3QsZW6rnOUEaiRUX6nCtA1v7abud1-4130_assertion description "[Norepinephrine transporter and catecholamine-O-methyltransferase gene variants and attention-deficit/hyperactivity disorder symptoms in adults.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP115066.RANOVZTCm0vFdF3QsZW6rnOUEaiRUX6nCtA1v7abud1-4130_provenance.
- NP115066.RANOVZTCm0vFdF3QsZW6rnOUEaiRUX6nCtA1v7abud1-4130_assertion evidence source_evidence_literature NP115066.RANOVZTCm0vFdF3QsZW6rnOUEaiRUX6nCtA1v7abud1-4130_provenance.
- NP115066.RANOVZTCm0vFdF3QsZW6rnOUEaiRUX6nCtA1v7abud1-4130_assertion SIO_000772 17994190 NP115066.RANOVZTCm0vFdF3QsZW6rnOUEaiRUX6nCtA1v7abud1-4130_provenance.
- NP115066.RANOVZTCm0vFdF3QsZW6rnOUEaiRUX6nCtA1v7abud1-4130_assertion wasDerivedFrom gad-20150221 NP115066.RANOVZTCm0vFdF3QsZW6rnOUEaiRUX6nCtA1v7abud1-4130_provenance.
- NP115066.RANOVZTCm0vFdF3QsZW6rnOUEaiRUX6nCtA1v7abud1-4130_assertion wasGeneratedBy ECO_0000203 NP115066.RANOVZTCm0vFdF3QsZW6rnOUEaiRUX6nCtA1v7abud1-4130_provenance.
- gad-20150221 importedOn "2015-02-21" NP115066.RANOVZTCm0vFdF3QsZW6rnOUEaiRUX6nCtA1v7abud1-4130_provenance.