Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP308938.RALmCxUEnVyYDrVKR-vO0jGPBRDV1V6HH2ccqGmeoiQrU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP308938.RALmCxUEnVyYDrVKR-vO0jGPBRDV1V6HH2ccqGmeoiQrU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP308938.RALmCxUEnVyYDrVKR-vO0jGPBRDV1V6HH2ccqGmeoiQrU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP308938.RALmCxUEnVyYDrVKR-vO0jGPBRDV1V6HH2ccqGmeoiQrU130_provenance.
- NP308938.RALmCxUEnVyYDrVKR-vO0jGPBRDV1V6HH2ccqGmeoiQrU130_assertion description "[In this study, we scanned the coding region of the PACAP gene for mutations in 24 Japanese patients with schizophrenia and 24 Japanese patients with bipolar disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP308938.RALmCxUEnVyYDrVKR-vO0jGPBRDV1V6HH2ccqGmeoiQrU130_provenance.
- NP308938.RALmCxUEnVyYDrVKR-vO0jGPBRDV1V6HH2ccqGmeoiQrU130_assertion evidence source_evidence_literature NP308938.RALmCxUEnVyYDrVKR-vO0jGPBRDV1V6HH2ccqGmeoiQrU130_provenance.
- NP308938.RALmCxUEnVyYDrVKR-vO0jGPBRDV1V6HH2ccqGmeoiQrU130_assertion SIO_000772 11515750 NP308938.RALmCxUEnVyYDrVKR-vO0jGPBRDV1V6HH2ccqGmeoiQrU130_provenance.
- NP308938.RALmCxUEnVyYDrVKR-vO0jGPBRDV1V6HH2ccqGmeoiQrU130_assertion wasDerivedFrom befree-20140225 NP308938.RALmCxUEnVyYDrVKR-vO0jGPBRDV1V6HH2ccqGmeoiQrU130_provenance.
- NP308938.RALmCxUEnVyYDrVKR-vO0jGPBRDV1V6HH2ccqGmeoiQrU130_assertion wasGeneratedBy ECO_0000203 NP308938.RALmCxUEnVyYDrVKR-vO0jGPBRDV1V6HH2ccqGmeoiQrU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP308938.RALmCxUEnVyYDrVKR-vO0jGPBRDV1V6HH2ccqGmeoiQrU130_provenance.