Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP263793.RA3UKYBch5qh5wJHGNckj4R0l0glmA1K5Bhl5PxvWbAHo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP263793.RA3UKYBch5qh5wJHGNckj4R0l0glmA1K5Bhl5PxvWbAHo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP263793.RA3UKYBch5qh5wJHGNckj4R0l0glmA1K5Bhl5PxvWbAHo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP263793.RA3UKYBch5qh5wJHGNckj4R0l0glmA1K5Bhl5PxvWbAHo130_provenance.
- NP263793.RA3UKYBch5qh5wJHGNckj4R0l0glmA1K5Bhl5PxvWbAHo130_assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP263793.RA3UKYBch5qh5wJHGNckj4R0l0glmA1K5Bhl5PxvWbAHo130_provenance.
- NP263793.RA3UKYBch5qh5wJHGNckj4R0l0glmA1K5Bhl5PxvWbAHo130_assertion evidence source_evidence_literature NP263793.RA3UKYBch5qh5wJHGNckj4R0l0glmA1K5Bhl5PxvWbAHo130_provenance.
- NP263793.RA3UKYBch5qh5wJHGNckj4R0l0glmA1K5Bhl5PxvWbAHo130_assertion SIO_000772 10496225 NP263793.RA3UKYBch5qh5wJHGNckj4R0l0glmA1K5Bhl5PxvWbAHo130_provenance.
- NP263793.RA3UKYBch5qh5wJHGNckj4R0l0glmA1K5Bhl5PxvWbAHo130_assertion wasDerivedFrom befree-2016 NP263793.RA3UKYBch5qh5wJHGNckj4R0l0glmA1K5Bhl5PxvWbAHo130_provenance.
- NP263793.RA3UKYBch5qh5wJHGNckj4R0l0glmA1K5Bhl5PxvWbAHo130_assertion wasGeneratedBy ECO_0000203 NP263793.RA3UKYBch5qh5wJHGNckj4R0l0glmA1K5Bhl5PxvWbAHo130_provenance.
- befree-2016 importedOn "2016-02-19" NP263793.RA3UKYBch5qh5wJHGNckj4R0l0glmA1K5Bhl5PxvWbAHo130_provenance.