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- source_evidence_literature type ECO_0000212 NP1066301.RABoTqzRKCTpvuarDUwXqTIxlN3U-MRrhueDxF112Tv04130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1066301.RABoTqzRKCTpvuarDUwXqTIxlN3U-MRrhueDxF112Tv04130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1066301.RABoTqzRKCTpvuarDUwXqTIxlN3U-MRrhueDxF112Tv04130_provenance.
- NP1066301.RABoTqzRKCTpvuarDUwXqTIxlN3U-MRrhueDxF112Tv04130_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." NP1066301.RABoTqzRKCTpvuarDUwXqTIxlN3U-MRrhueDxF112Tv04130_provenance.
- NP1066301.RABoTqzRKCTpvuarDUwXqTIxlN3U-MRrhueDxF112Tv04130_assertion evidence source_evidence_literature NP1066301.RABoTqzRKCTpvuarDUwXqTIxlN3U-MRrhueDxF112Tv04130_provenance.
- NP1066301.RABoTqzRKCTpvuarDUwXqTIxlN3U-MRrhueDxF112Tv04130_assertion SIO_000772 23555284 NP1066301.RABoTqzRKCTpvuarDUwXqTIxlN3U-MRrhueDxF112Tv04130_provenance.
- NP1066301.RABoTqzRKCTpvuarDUwXqTIxlN3U-MRrhueDxF112Tv04130_assertion wasDerivedFrom befree-2016 NP1066301.RABoTqzRKCTpvuarDUwXqTIxlN3U-MRrhueDxF112Tv04130_provenance.
- NP1066301.RABoTqzRKCTpvuarDUwXqTIxlN3U-MRrhueDxF112Tv04130_assertion wasGeneratedBy ECO_0000203 NP1066301.RABoTqzRKCTpvuarDUwXqTIxlN3U-MRrhueDxF112Tv04130_provenance.
- befree-2016 importedOn "2016-02-19" NP1066301.RABoTqzRKCTpvuarDUwXqTIxlN3U-MRrhueDxF112Tv04130_provenance.