Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP856626.RAfgo4BOm5ShJq8XeXWcNYf5priRWRSMSfCgtMU-E79Fg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP856626.RAfgo4BOm5ShJq8XeXWcNYf5priRWRSMSfCgtMU-E79Fg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP856626.RAfgo4BOm5ShJq8XeXWcNYf5priRWRSMSfCgtMU-E79Fg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP856626.RAfgo4BOm5ShJq8XeXWcNYf5priRWRSMSfCgtMU-E79Fg130_provenance.
- NP856626.RAfgo4BOm5ShJq8XeXWcNYf5priRWRSMSfCgtMU-E79Fg130_assertion description "[GEP NETs occur either sporadically or as part of endocrine tumor susceptibility syndromes such as multiple endocrine neoplasia type 1 (MEN1), von Hippel Lindau (VHL) syndrome, neurofibromatosis (NF-1), and possibly tuberous sclerosis (TSC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP856626.RAfgo4BOm5ShJq8XeXWcNYf5priRWRSMSfCgtMU-E79Fg130_provenance.
- NP856626.RAfgo4BOm5ShJq8XeXWcNYf5priRWRSMSfCgtMU-E79Fg130_assertion evidence source_evidence_literature NP856626.RAfgo4BOm5ShJq8XeXWcNYf5priRWRSMSfCgtMU-E79Fg130_provenance.
- NP856626.RAfgo4BOm5ShJq8XeXWcNYf5priRWRSMSfCgtMU-E79Fg130_assertion SIO_000772 19125015 NP856626.RAfgo4BOm5ShJq8XeXWcNYf5priRWRSMSfCgtMU-E79Fg130_provenance.
- NP856626.RAfgo4BOm5ShJq8XeXWcNYf5priRWRSMSfCgtMU-E79Fg130_assertion wasDerivedFrom befree-20140225 NP856626.RAfgo4BOm5ShJq8XeXWcNYf5priRWRSMSfCgtMU-E79Fg130_provenance.
- NP856626.RAfgo4BOm5ShJq8XeXWcNYf5priRWRSMSfCgtMU-E79Fg130_assertion wasGeneratedBy ECO_0000203 NP856626.RAfgo4BOm5ShJq8XeXWcNYf5priRWRSMSfCgtMU-E79Fg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP856626.RAfgo4BOm5ShJq8XeXWcNYf5priRWRSMSfCgtMU-E79Fg130_provenance.