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- source_evidence_literature type ECO_0000212 NP867501.RAwx_uO9JWRAlK-4uA9cCD-pEneryp9Pa-QivvPSE1syI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP867501.RAwx_uO9JWRAlK-4uA9cCD-pEneryp9Pa-QivvPSE1syI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP867501.RAwx_uO9JWRAlK-4uA9cCD-pEneryp9Pa-QivvPSE1syI130_provenance.
- NP867501.RAwx_uO9JWRAlK-4uA9cCD-pEneryp9Pa-QivvPSE1syI130_assertion description "[Together, these results support a model where the DIA1 and DIA1R gene products regulate molecular traffic through the cellular secretory pathway or affect the function of secreted factors, and functional deficits cause disorders with ASD-like symptoms and/or mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP867501.RAwx_uO9JWRAlK-4uA9cCD-pEneryp9Pa-QivvPSE1syI130_provenance.
- NP867501.RAwx_uO9JWRAlK-4uA9cCD-pEneryp9Pa-QivvPSE1syI130_assertion evidence source_evidence_literature NP867501.RAwx_uO9JWRAlK-4uA9cCD-pEneryp9Pa-QivvPSE1syI130_provenance.
- NP867501.RAwx_uO9JWRAlK-4uA9cCD-pEneryp9Pa-QivvPSE1syI130_assertion SIO_000772 21264219 NP867501.RAwx_uO9JWRAlK-4uA9cCD-pEneryp9Pa-QivvPSE1syI130_provenance.
- NP867501.RAwx_uO9JWRAlK-4uA9cCD-pEneryp9Pa-QivvPSE1syI130_assertion wasDerivedFrom befree-2016 NP867501.RAwx_uO9JWRAlK-4uA9cCD-pEneryp9Pa-QivvPSE1syI130_provenance.
- NP867501.RAwx_uO9JWRAlK-4uA9cCD-pEneryp9Pa-QivvPSE1syI130_assertion wasGeneratedBy ECO_0000203 NP867501.RAwx_uO9JWRAlK-4uA9cCD-pEneryp9Pa-QivvPSE1syI130_provenance.
- befree-2016 importedOn "2016-02-19" NP867501.RAwx_uO9JWRAlK-4uA9cCD-pEneryp9Pa-QivvPSE1syI130_provenance.