Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP553463.RAM091WVyTAQmxTCnHuwRWS6EaS-RdZuuz_rp5SFwPlHs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP553463.RAM091WVyTAQmxTCnHuwRWS6EaS-RdZuuz_rp5SFwPlHs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP553463.RAM091WVyTAQmxTCnHuwRWS6EaS-RdZuuz_rp5SFwPlHs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP553463.RAM091WVyTAQmxTCnHuwRWS6EaS-RdZuuz_rp5SFwPlHs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP553463.RAM091WVyTAQmxTCnHuwRWS6EaS-RdZuuz_rp5SFwPlHs130_provenance.
- NP553463.RAM091WVyTAQmxTCnHuwRWS6EaS-RdZuuz_rp5SFwPlHs130_assertion wasGeneratedBy ECO_0000203 NP553463.RAM091WVyTAQmxTCnHuwRWS6EaS-RdZuuz_rp5SFwPlHs130_provenance.
- NP553463.RAM091WVyTAQmxTCnHuwRWS6EaS-RdZuuz_rp5SFwPlHs130_assertion wasDerivedFrom befree-20150227 NP553463.RAM091WVyTAQmxTCnHuwRWS6EaS-RdZuuz_rp5SFwPlHs130_provenance.
- NP553463.RAM091WVyTAQmxTCnHuwRWS6EaS-RdZuuz_rp5SFwPlHs130_assertion SIO_000772 22009375 NP553463.RAM091WVyTAQmxTCnHuwRWS6EaS-RdZuuz_rp5SFwPlHs130_provenance.
- NP553463.RAM091WVyTAQmxTCnHuwRWS6EaS-RdZuuz_rp5SFwPlHs130_assertion evidence source_evidence_literature NP553463.RAM091WVyTAQmxTCnHuwRWS6EaS-RdZuuz_rp5SFwPlHs130_provenance.
- NP553463.RAM091WVyTAQmxTCnHuwRWS6EaS-RdZuuz_rp5SFwPlHs130_assertion description "[46 subjects referred for hereditary NET syndrome [22 MEN1, 12 MEN2, 12 Familial Paragangliomatosis (FPGL)] were enrolled and divided in 2 groups (group A, 20 subjects with clinical appearance of NET before the genetic diagnosis; group B, 26 subjects with genetic diagnosis of hereditary NET syndromes before the clinical appearance of NETs).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP553463.RAM091WVyTAQmxTCnHuwRWS6EaS-RdZuuz_rp5SFwPlHs130_provenance.