Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP931173.RAuWpmXINCZ2RB9ru3PTz8cI1W3z_moEF1NXRunEiXCK4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP931173.RAuWpmXINCZ2RB9ru3PTz8cI1W3z_moEF1NXRunEiXCK4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP931173.RAuWpmXINCZ2RB9ru3PTz8cI1W3z_moEF1NXRunEiXCK4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP931173.RAuWpmXINCZ2RB9ru3PTz8cI1W3z_moEF1NXRunEiXCK4130_provenance.
- NP931173.RAuWpmXINCZ2RB9ru3PTz8cI1W3z_moEF1NXRunEiXCK4130_assertion description "[The role of the fragile X mental retardation protein (FMRP) is well established in brain, where its absence leads to the fragile X syndrome (FXS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP931173.RAuWpmXINCZ2RB9ru3PTz8cI1W3z_moEF1NXRunEiXCK4130_provenance.
- NP931173.RAuWpmXINCZ2RB9ru3PTz8cI1W3z_moEF1NXRunEiXCK4130_assertion evidence source_evidence_literature NP931173.RAuWpmXINCZ2RB9ru3PTz8cI1W3z_moEF1NXRunEiXCK4130_provenance.
- NP931173.RAuWpmXINCZ2RB9ru3PTz8cI1W3z_moEF1NXRunEiXCK4130_assertion SIO_000772 24092663 NP931173.RAuWpmXINCZ2RB9ru3PTz8cI1W3z_moEF1NXRunEiXCK4130_provenance.
- NP931173.RAuWpmXINCZ2RB9ru3PTz8cI1W3z_moEF1NXRunEiXCK4130_assertion wasDerivedFrom befree-20150227 NP931173.RAuWpmXINCZ2RB9ru3PTz8cI1W3z_moEF1NXRunEiXCK4130_provenance.
- NP931173.RAuWpmXINCZ2RB9ru3PTz8cI1W3z_moEF1NXRunEiXCK4130_assertion wasGeneratedBy ECO_0000203 NP931173.RAuWpmXINCZ2RB9ru3PTz8cI1W3z_moEF1NXRunEiXCK4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP931173.RAuWpmXINCZ2RB9ru3PTz8cI1W3z_moEF1NXRunEiXCK4130_provenance.