Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP682281.RACmeoxg3YLpP6UcQh8LRFpirLGAiWFWPXz1NHB4Txm2Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP682281.RACmeoxg3YLpP6UcQh8LRFpirLGAiWFWPXz1NHB4Txm2Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP682281.RACmeoxg3YLpP6UcQh8LRFpirLGAiWFWPXz1NHB4Txm2Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP682281.RACmeoxg3YLpP6UcQh8LRFpirLGAiWFWPXz1NHB4Txm2Y130_provenance.
- befree-2016 importedOn "2016-02-19" NP682281.RACmeoxg3YLpP6UcQh8LRFpirLGAiWFWPXz1NHB4Txm2Y130_provenance.
- NP682281.RACmeoxg3YLpP6UcQh8LRFpirLGAiWFWPXz1NHB4Txm2Y130_assertion wasGeneratedBy ECO_0000203 NP682281.RACmeoxg3YLpP6UcQh8LRFpirLGAiWFWPXz1NHB4Txm2Y130_provenance.
- NP682281.RACmeoxg3YLpP6UcQh8LRFpirLGAiWFWPXz1NHB4Txm2Y130_assertion wasDerivedFrom befree-2016 NP682281.RACmeoxg3YLpP6UcQh8LRFpirLGAiWFWPXz1NHB4Txm2Y130_provenance.
- NP682281.RACmeoxg3YLpP6UcQh8LRFpirLGAiWFWPXz1NHB4Txm2Y130_assertion SIO_000772 18628314 NP682281.RACmeoxg3YLpP6UcQh8LRFpirLGAiWFWPXz1NHB4Txm2Y130_provenance.
- NP682281.RACmeoxg3YLpP6UcQh8LRFpirLGAiWFWPXz1NHB4Txm2Y130_assertion evidence source_evidence_literature NP682281.RACmeoxg3YLpP6UcQh8LRFpirLGAiWFWPXz1NHB4Txm2Y130_provenance.
- NP682281.RACmeoxg3YLpP6UcQh8LRFpirLGAiWFWPXz1NHB4Txm2Y130_assertion description "[The Fragile X Mental retardation-Related 1 (FXR1) gene belongs to the fragile X related family, that also includes the Fragile X Mental Retardation (FMR1) gene involved in fragile X syndrome, the most common form of inherited mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682281.RACmeoxg3YLpP6UcQh8LRFpirLGAiWFWPXz1NHB4Txm2Y130_provenance.