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- source_evidence_literature type ECO_0000212 NP409136.RAbtSRkyrnPuN9iSAs-vyypqoldIngvjjxZ32eU8rbklQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP409136.RAbtSRkyrnPuN9iSAs-vyypqoldIngvjjxZ32eU8rbklQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP409136.RAbtSRkyrnPuN9iSAs-vyypqoldIngvjjxZ32eU8rbklQ130_provenance.
- NP409136.RAbtSRkyrnPuN9iSAs-vyypqoldIngvjjxZ32eU8rbklQ130_assertion description "[The Fragile X-Related 1 gene (FXR1) is a paralog of the Fragile X Mental Retardation 1 gene (FMR1), whose absence causes the Fragile X syndrome, the most common form of inherited intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP409136.RAbtSRkyrnPuN9iSAs-vyypqoldIngvjjxZ32eU8rbklQ130_provenance.
- NP409136.RAbtSRkyrnPuN9iSAs-vyypqoldIngvjjxZ32eU8rbklQ130_assertion evidence source_evidence_literature NP409136.RAbtSRkyrnPuN9iSAs-vyypqoldIngvjjxZ32eU8rbklQ130_provenance.
- NP409136.RAbtSRkyrnPuN9iSAs-vyypqoldIngvjjxZ32eU8rbklQ130_assertion SIO_000772 23555284 NP409136.RAbtSRkyrnPuN9iSAs-vyypqoldIngvjjxZ32eU8rbklQ130_provenance.
- NP409136.RAbtSRkyrnPuN9iSAs-vyypqoldIngvjjxZ32eU8rbklQ130_assertion wasDerivedFrom befree-20150227 NP409136.RAbtSRkyrnPuN9iSAs-vyypqoldIngvjjxZ32eU8rbklQ130_provenance.
- NP409136.RAbtSRkyrnPuN9iSAs-vyypqoldIngvjjxZ32eU8rbklQ130_assertion wasGeneratedBy ECO_0000203 NP409136.RAbtSRkyrnPuN9iSAs-vyypqoldIngvjjxZ32eU8rbklQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP409136.RAbtSRkyrnPuN9iSAs-vyypqoldIngvjjxZ32eU8rbklQ130_provenance.