Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP362234.RALYvHi3cHO50hc1SUsZGcMNW9x0f4FAaQffNyTYn13tQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP362234.RALYvHi3cHO50hc1SUsZGcMNW9x0f4FAaQffNyTYn13tQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP362234.RALYvHi3cHO50hc1SUsZGcMNW9x0f4FAaQffNyTYn13tQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP362234.RALYvHi3cHO50hc1SUsZGcMNW9x0f4FAaQffNyTYn13tQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP362234.RALYvHi3cHO50hc1SUsZGcMNW9x0f4FAaQffNyTYn13tQ130_provenance.
- NP362234.RALYvHi3cHO50hc1SUsZGcMNW9x0f4FAaQffNyTYn13tQ130_assertion wasGeneratedBy ECO_0000203 NP362234.RALYvHi3cHO50hc1SUsZGcMNW9x0f4FAaQffNyTYn13tQ130_provenance.
- NP362234.RALYvHi3cHO50hc1SUsZGcMNW9x0f4FAaQffNyTYn13tQ130_assertion wasDerivedFrom befree-2016 NP362234.RALYvHi3cHO50hc1SUsZGcMNW9x0f4FAaQffNyTYn13tQ130_provenance.
- NP362234.RALYvHi3cHO50hc1SUsZGcMNW9x0f4FAaQffNyTYn13tQ130_assertion SIO_000772 12135967 NP362234.RALYvHi3cHO50hc1SUsZGcMNW9x0f4FAaQffNyTYn13tQ130_provenance.
- NP362234.RALYvHi3cHO50hc1SUsZGcMNW9x0f4FAaQffNyTYn13tQ130_assertion evidence source_evidence_literature NP362234.RALYvHi3cHO50hc1SUsZGcMNW9x0f4FAaQffNyTYn13tQ130_provenance.
- NP362234.RALYvHi3cHO50hc1SUsZGcMNW9x0f4FAaQffNyTYn13tQ130_assertion description "[The presence of inclusions in the brains of all four FXS carriers with the neurological findings provides further support for a unique clinical entity associated with pre-mutation FMR1 alleles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP362234.RALYvHi3cHO50hc1SUsZGcMNW9x0f4FAaQffNyTYn13tQ130_provenance.