Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP418721.RACiNDd08qUYWYqqbRcbQFuUvJ68ZP3ApPVR6dGP_KXoE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP418721.RACiNDd08qUYWYqqbRcbQFuUvJ68ZP3ApPVR6dGP_KXoE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP418721.RACiNDd08qUYWYqqbRcbQFuUvJ68ZP3ApPVR6dGP_KXoE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP418721.RACiNDd08qUYWYqqbRcbQFuUvJ68ZP3ApPVR6dGP_KXoE130_provenance.
- NP418721.RACiNDd08qUYWYqqbRcbQFuUvJ68ZP3ApPVR6dGP_KXoE130_assertion description "[Certain patients with apparently sporadic parathyroid carcinoma carry germ-line mutations in HRPT2 and may have the HPT-JT syndrome or a phenotypic variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418721.RACiNDd08qUYWYqqbRcbQFuUvJ68ZP3ApPVR6dGP_KXoE130_provenance.
- NP418721.RACiNDd08qUYWYqqbRcbQFuUvJ68ZP3ApPVR6dGP_KXoE130_assertion evidence source_evidence_literature NP418721.RACiNDd08qUYWYqqbRcbQFuUvJ68ZP3ApPVR6dGP_KXoE130_provenance.
- NP418721.RACiNDd08qUYWYqqbRcbQFuUvJ68ZP3ApPVR6dGP_KXoE130_assertion SIO_000772 14585940 NP418721.RACiNDd08qUYWYqqbRcbQFuUvJ68ZP3ApPVR6dGP_KXoE130_provenance.
- NP418721.RACiNDd08qUYWYqqbRcbQFuUvJ68ZP3ApPVR6dGP_KXoE130_assertion wasDerivedFrom befree-2016 NP418721.RACiNDd08qUYWYqqbRcbQFuUvJ68ZP3ApPVR6dGP_KXoE130_provenance.
- NP418721.RACiNDd08qUYWYqqbRcbQFuUvJ68ZP3ApPVR6dGP_KXoE130_assertion wasGeneratedBy ECO_0000203 NP418721.RACiNDd08qUYWYqqbRcbQFuUvJ68ZP3ApPVR6dGP_KXoE130_provenance.
- befree-2016 importedOn "2016-02-19" NP418721.RACiNDd08qUYWYqqbRcbQFuUvJ68ZP3ApPVR6dGP_KXoE130_provenance.