Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP258809.RA5z2_3D00BGBA7U1QPrtHSisxoOQYMAR5bTD4e0i72Fg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP258809.RA5z2_3D00BGBA7U1QPrtHSisxoOQYMAR5bTD4e0i72Fg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP258809.RA5z2_3D00BGBA7U1QPrtHSisxoOQYMAR5bTD4e0i72Fg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP258809.RA5z2_3D00BGBA7U1QPrtHSisxoOQYMAR5bTD4e0i72Fg130_provenance.
- befree-2016 importedOn "2016-02-19" NP258809.RA5z2_3D00BGBA7U1QPrtHSisxoOQYMAR5bTD4e0i72Fg130_provenance.
- NP258809.RA5z2_3D00BGBA7U1QPrtHSisxoOQYMAR5bTD4e0i72Fg130_assertion wasGeneratedBy ECO_0000203 NP258809.RA5z2_3D00BGBA7U1QPrtHSisxoOQYMAR5bTD4e0i72Fg130_provenance.
- NP258809.RA5z2_3D00BGBA7U1QPrtHSisxoOQYMAR5bTD4e0i72Fg130_assertion wasDerivedFrom befree-2016 NP258809.RA5z2_3D00BGBA7U1QPrtHSisxoOQYMAR5bTD4e0i72Fg130_provenance.
- NP258809.RA5z2_3D00BGBA7U1QPrtHSisxoOQYMAR5bTD4e0i72Fg130_assertion SIO_000772 10424820 NP258809.RA5z2_3D00BGBA7U1QPrtHSisxoOQYMAR5bTD4e0i72Fg130_provenance.
- NP258809.RA5z2_3D00BGBA7U1QPrtHSisxoOQYMAR5bTD4e0i72Fg130_assertion evidence source_evidence_literature NP258809.RA5z2_3D00BGBA7U1QPrtHSisxoOQYMAR5bTD4e0i72Fg130_provenance.
- NP258809.RA5z2_3D00BGBA7U1QPrtHSisxoOQYMAR5bTD4e0i72Fg130_assertion description "[Fragile X syndrome with FMR1 and FMR2 deletion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP258809.RA5z2_3D00BGBA7U1QPrtHSisxoOQYMAR5bTD4e0i72Fg130_provenance.