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- source_evidence_literature type ECO_0000212 NP433873.RAkodiA-kz4NyMi9l-CPCvkq1QknHmU_a20ekOs-zzCVU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP433873.RAkodiA-kz4NyMi9l-CPCvkq1QknHmU_a20ekOs-zzCVU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP433873.RAkodiA-kz4NyMi9l-CPCvkq1QknHmU_a20ekOs-zzCVU130_provenance.
- NP433873.RAkodiA-kz4NyMi9l-CPCvkq1QknHmU_a20ekOs-zzCVU130_assertion description "[Exploring the potential role of disease-causing mutation in a gene desert: duplication of noncoding elements 5' of GRIA3 is associated with GRIA3 silencing and X-linked intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP433873.RAkodiA-kz4NyMi9l-CPCvkq1QknHmU_a20ekOs-zzCVU130_provenance.
- NP433873.RAkodiA-kz4NyMi9l-CPCvkq1QknHmU_a20ekOs-zzCVU130_assertion evidence source_evidence_literature NP433873.RAkodiA-kz4NyMi9l-CPCvkq1QknHmU_a20ekOs-zzCVU130_provenance.
- NP433873.RAkodiA-kz4NyMi9l-CPCvkq1QknHmU_a20ekOs-zzCVU130_assertion SIO_000772 22124977 NP433873.RAkodiA-kz4NyMi9l-CPCvkq1QknHmU_a20ekOs-zzCVU130_provenance.
- NP433873.RAkodiA-kz4NyMi9l-CPCvkq1QknHmU_a20ekOs-zzCVU130_assertion wasDerivedFrom befree-20150227 NP433873.RAkodiA-kz4NyMi9l-CPCvkq1QknHmU_a20ekOs-zzCVU130_provenance.
- NP433873.RAkodiA-kz4NyMi9l-CPCvkq1QknHmU_a20ekOs-zzCVU130_assertion wasGeneratedBy ECO_0000203 NP433873.RAkodiA-kz4NyMi9l-CPCvkq1QknHmU_a20ekOs-zzCVU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP433873.RAkodiA-kz4NyMi9l-CPCvkq1QknHmU_a20ekOs-zzCVU130_provenance.