Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP789966.RAAHoA-OgWQNhiVlLVkxvjKMU58iKzzAEoDj7JqG_Freg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP789966.RAAHoA-OgWQNhiVlLVkxvjKMU58iKzzAEoDj7JqG_Freg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP789966.RAAHoA-OgWQNhiVlLVkxvjKMU58iKzzAEoDj7JqG_Freg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP789966.RAAHoA-OgWQNhiVlLVkxvjKMU58iKzzAEoDj7JqG_Freg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP789966.RAAHoA-OgWQNhiVlLVkxvjKMU58iKzzAEoDj7JqG_Freg130_provenance.
- NP789966.RAAHoA-OgWQNhiVlLVkxvjKMU58iKzzAEoDj7JqG_Freg130_assertion wasGeneratedBy ECO_0000203 NP789966.RAAHoA-OgWQNhiVlLVkxvjKMU58iKzzAEoDj7JqG_Freg130_provenance.
- NP789966.RAAHoA-OgWQNhiVlLVkxvjKMU58iKzzAEoDj7JqG_Freg130_assertion wasDerivedFrom befree-20150227 NP789966.RAAHoA-OgWQNhiVlLVkxvjKMU58iKzzAEoDj7JqG_Freg130_provenance.
- NP789966.RAAHoA-OgWQNhiVlLVkxvjKMU58iKzzAEoDj7JqG_Freg130_assertion SIO_000772 18628314 NP789966.RAAHoA-OgWQNhiVlLVkxvjKMU58iKzzAEoDj7JqG_Freg130_provenance.
- NP789966.RAAHoA-OgWQNhiVlLVkxvjKMU58iKzzAEoDj7JqG_Freg130_assertion evidence source_evidence_literature NP789966.RAAHoA-OgWQNhiVlLVkxvjKMU58iKzzAEoDj7JqG_Freg130_provenance.
- NP789966.RAAHoA-OgWQNhiVlLVkxvjKMU58iKzzAEoDj7JqG_Freg130_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." NP789966.RAAHoA-OgWQNhiVlLVkxvjKMU58iKzzAEoDj7JqG_Freg130_provenance.