Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP553314.RAoVLt6Vd5xklC9MUaCa7DQdNySCrWc_gTv21e_MnRhwY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP553314.RAoVLt6Vd5xklC9MUaCa7DQdNySCrWc_gTv21e_MnRhwY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP553314.RAoVLt6Vd5xklC9MUaCa7DQdNySCrWc_gTv21e_MnRhwY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP553314.RAoVLt6Vd5xklC9MUaCa7DQdNySCrWc_gTv21e_MnRhwY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP553314.RAoVLt6Vd5xklC9MUaCa7DQdNySCrWc_gTv21e_MnRhwY130_provenance.
- NP553314.RAoVLt6Vd5xklC9MUaCa7DQdNySCrWc_gTv21e_MnRhwY130_assertion wasGeneratedBy ECO_0000203 NP553314.RAoVLt6Vd5xklC9MUaCa7DQdNySCrWc_gTv21e_MnRhwY130_provenance.
- NP553314.RAoVLt6Vd5xklC9MUaCa7DQdNySCrWc_gTv21e_MnRhwY130_assertion wasDerivedFrom befree-20150227 NP553314.RAoVLt6Vd5xklC9MUaCa7DQdNySCrWc_gTv21e_MnRhwY130_provenance.
- NP553314.RAoVLt6Vd5xklC9MUaCa7DQdNySCrWc_gTv21e_MnRhwY130_assertion SIO_000772 22846739 NP553314.RAoVLt6Vd5xklC9MUaCa7DQdNySCrWc_gTv21e_MnRhwY130_provenance.
- NP553314.RAoVLt6Vd5xklC9MUaCa7DQdNySCrWc_gTv21e_MnRhwY130_assertion evidence source_evidence_literature NP553314.RAoVLt6Vd5xklC9MUaCa7DQdNySCrWc_gTv21e_MnRhwY130_provenance.
- NP553314.RAoVLt6Vd5xklC9MUaCa7DQdNySCrWc_gTv21e_MnRhwY130_assertion description "[The primary syndromes (and genes) addressed here include multiple endocrine neoplasia types 1 and 2 (MEN1 and RET genes), Cowden syndrome (PTEN), hereditary pheochromocytoma/paraganglioma syndromes (multiple genes), and von Hippel-Lindau disease (VHL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP553314.RAoVLt6Vd5xklC9MUaCa7DQdNySCrWc_gTv21e_MnRhwY130_provenance.