Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP365960.RAGNSbfboy9-n90Iz5uy4BbCGUMIN0lR94fRPohZJdd5g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP365960.RAGNSbfboy9-n90Iz5uy4BbCGUMIN0lR94fRPohZJdd5g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP365960.RAGNSbfboy9-n90Iz5uy4BbCGUMIN0lR94fRPohZJdd5g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP365960.RAGNSbfboy9-n90Iz5uy4BbCGUMIN0lR94fRPohZJdd5g130_provenance.
- NP365960.RAGNSbfboy9-n90Iz5uy4BbCGUMIN0lR94fRPohZJdd5g130_assertion description "[FRAXE mental retardation, a recently identified rare genetic condition, is due to a mutation of the FMR2 gene, located at Xq28 region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP365960.RAGNSbfboy9-n90Iz5uy4BbCGUMIN0lR94fRPohZJdd5g130_provenance.
- NP365960.RAGNSbfboy9-n90Iz5uy4BbCGUMIN0lR94fRPohZJdd5g130_assertion evidence source_evidence_literature NP365960.RAGNSbfboy9-n90Iz5uy4BbCGUMIN0lR94fRPohZJdd5g130_provenance.
- NP365960.RAGNSbfboy9-n90Iz5uy4BbCGUMIN0lR94fRPohZJdd5g130_assertion SIO_000772 10964075 NP365960.RAGNSbfboy9-n90Iz5uy4BbCGUMIN0lR94fRPohZJdd5g130_provenance.
- NP365960.RAGNSbfboy9-n90Iz5uy4BbCGUMIN0lR94fRPohZJdd5g130_assertion wasDerivedFrom befree-20140225 NP365960.RAGNSbfboy9-n90Iz5uy4BbCGUMIN0lR94fRPohZJdd5g130_provenance.
- NP365960.RAGNSbfboy9-n90Iz5uy4BbCGUMIN0lR94fRPohZJdd5g130_assertion wasGeneratedBy ECO_0000203 NP365960.RAGNSbfboy9-n90Iz5uy4BbCGUMIN0lR94fRPohZJdd5g130_provenance.
- befree-20140225 importedOn "2014-02-25" NP365960.RAGNSbfboy9-n90Iz5uy4BbCGUMIN0lR94fRPohZJdd5g130_provenance.