Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP476016.RA8d01F18I8eAeBXe-pCKxorl2Wj5EaXlsGolS1-HdaxE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP476016.RA8d01F18I8eAeBXe-pCKxorl2Wj5EaXlsGolS1-HdaxE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP476016.RA8d01F18I8eAeBXe-pCKxorl2Wj5EaXlsGolS1-HdaxE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP476016.RA8d01F18I8eAeBXe-pCKxorl2Wj5EaXlsGolS1-HdaxE130_provenance.
- NP476016.RA8d01F18I8eAeBXe-pCKxorl2Wj5EaXlsGolS1-HdaxE130_assertion wasGeneratedBy ECO_0000203 NP476016.RA8d01F18I8eAeBXe-pCKxorl2Wj5EaXlsGolS1-HdaxE130_provenance.
- NP476016.RA8d01F18I8eAeBXe-pCKxorl2Wj5EaXlsGolS1-HdaxE130_assertion wasDerivedFrom befree-20140225 NP476016.RA8d01F18I8eAeBXe-pCKxorl2Wj5EaXlsGolS1-HdaxE130_provenance.
- NP476016.RA8d01F18I8eAeBXe-pCKxorl2Wj5EaXlsGolS1-HdaxE130_assertion SIO_000772 11562939 NP476016.RA8d01F18I8eAeBXe-pCKxorl2Wj5EaXlsGolS1-HdaxE130_provenance.
- NP476016.RA8d01F18I8eAeBXe-pCKxorl2Wj5EaXlsGolS1-HdaxE130_assertion evidence source_evidence_literature NP476016.RA8d01F18I8eAeBXe-pCKxorl2Wj5EaXlsGolS1-HdaxE130_provenance.
- NP476016.RA8d01F18I8eAeBXe-pCKxorl2Wj5EaXlsGolS1-HdaxE130_assertion description "[The search for targets of FMRP (the product of FMR1, the mutated gene in Fragile X syndrome) has predominantly focused on identifying transcripts that are regulated by this RNA-binding protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP476016.RA8d01F18I8eAeBXe-pCKxorl2Wj5EaXlsGolS1-HdaxE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP476016.RA8d01F18I8eAeBXe-pCKxorl2Wj5EaXlsGolS1-HdaxE130_provenance.