Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP718781.RA8QI5J5WwBPhiSsCwLm9cbEJjaAsr0Ah7PSZ5jB2PLGg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP718781.RA8QI5J5WwBPhiSsCwLm9cbEJjaAsr0Ah7PSZ5jB2PLGg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP718781.RA8QI5J5WwBPhiSsCwLm9cbEJjaAsr0Ah7PSZ5jB2PLGg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP718781.RA8QI5J5WwBPhiSsCwLm9cbEJjaAsr0Ah7PSZ5jB2PLGg130_provenance.
- NP718781.RA8QI5J5WwBPhiSsCwLm9cbEJjaAsr0Ah7PSZ5jB2PLGg130_assertion description "[Altogether eight abnormalities were repeatedly identified both as sole chromosomal anomalies and as part of more complex karyotypes: the structural rearrangements i(1)(q10), der(1:16)(q10;p10), del(1)(q11-12), del(3)(p12-13p14-21), and del(6)(q21-22) and the numerical aberrations +7, +18, and +20.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP718781.RA8QI5J5WwBPhiSsCwLm9cbEJjaAsr0Ah7PSZ5jB2PLGg130_provenance.
- NP718781.RA8QI5J5WwBPhiSsCwLm9cbEJjaAsr0Ah7PSZ5jB2PLGg130_assertion evidence source_evidence_literature NP718781.RA8QI5J5WwBPhiSsCwLm9cbEJjaAsr0Ah7PSZ5jB2PLGg130_provenance.
- NP718781.RA8QI5J5WwBPhiSsCwLm9cbEJjaAsr0Ah7PSZ5jB2PLGg130_assertion SIO_000772 7536456 NP718781.RA8QI5J5WwBPhiSsCwLm9cbEJjaAsr0Ah7PSZ5jB2PLGg130_provenance.
- NP718781.RA8QI5J5WwBPhiSsCwLm9cbEJjaAsr0Ah7PSZ5jB2PLGg130_assertion wasDerivedFrom befree-20140225 NP718781.RA8QI5J5WwBPhiSsCwLm9cbEJjaAsr0Ah7PSZ5jB2PLGg130_provenance.
- NP718781.RA8QI5J5WwBPhiSsCwLm9cbEJjaAsr0Ah7PSZ5jB2PLGg130_assertion wasGeneratedBy ECO_0000203 NP718781.RA8QI5J5WwBPhiSsCwLm9cbEJjaAsr0Ah7PSZ5jB2PLGg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP718781.RA8QI5J5WwBPhiSsCwLm9cbEJjaAsr0Ah7PSZ5jB2PLGg130_provenance.