Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP508329.RAfZc08R0nGffKe-QtN_3Ovg4bgTzGSWBVAJqM8sS5v9o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP508329.RAfZc08R0nGffKe-QtN_3Ovg4bgTzGSWBVAJqM8sS5v9o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP508329.RAfZc08R0nGffKe-QtN_3Ovg4bgTzGSWBVAJqM8sS5v9o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP508329.RAfZc08R0nGffKe-QtN_3Ovg4bgTzGSWBVAJqM8sS5v9o130_provenance.
- NP508329.RAfZc08R0nGffKe-QtN_3Ovg4bgTzGSWBVAJqM8sS5v9o130_assertion description "[MTC occurs in both sporadic and familial forms, the latter making up 25% of all MTCs and being comprised of three distinct syndromes--multiple endocrine neoplasia type 2A (MEN 2A), multiple endocrine neoplasia type 2B (MEN 2B), and familial medullary thyroid carcinoma (FMTC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP508329.RAfZc08R0nGffKe-QtN_3Ovg4bgTzGSWBVAJqM8sS5v9o130_provenance.
- NP508329.RAfZc08R0nGffKe-QtN_3Ovg4bgTzGSWBVAJqM8sS5v9o130_assertion evidence source_evidence_literature NP508329.RAfZc08R0nGffKe-QtN_3Ovg4bgTzGSWBVAJqM8sS5v9o130_provenance.
- NP508329.RAfZc08R0nGffKe-QtN_3Ovg4bgTzGSWBVAJqM8sS5v9o130_assertion SIO_000772 8563482 NP508329.RAfZc08R0nGffKe-QtN_3Ovg4bgTzGSWBVAJqM8sS5v9o130_provenance.
- NP508329.RAfZc08R0nGffKe-QtN_3Ovg4bgTzGSWBVAJqM8sS5v9o130_assertion wasDerivedFrom befree-20140225 NP508329.RAfZc08R0nGffKe-QtN_3Ovg4bgTzGSWBVAJqM8sS5v9o130_provenance.
- NP508329.RAfZc08R0nGffKe-QtN_3Ovg4bgTzGSWBVAJqM8sS5v9o130_assertion wasGeneratedBy ECO_0000203 NP508329.RAfZc08R0nGffKe-QtN_3Ovg4bgTzGSWBVAJqM8sS5v9o130_provenance.
- befree-20140225 importedOn "2014-02-25" NP508329.RAfZc08R0nGffKe-QtN_3Ovg4bgTzGSWBVAJqM8sS5v9o130_provenance.