Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP434546.RA7wYT2Th6ApSaL0d6sovUZslWnc2npTdYOVEtPQEudyI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP434546.RA7wYT2Th6ApSaL0d6sovUZslWnc2npTdYOVEtPQEudyI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP434546.RA7wYT2Th6ApSaL0d6sovUZslWnc2npTdYOVEtPQEudyI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP434546.RA7wYT2Th6ApSaL0d6sovUZslWnc2npTdYOVEtPQEudyI130_provenance.
- NP434546.RA7wYT2Th6ApSaL0d6sovUZslWnc2npTdYOVEtPQEudyI130_assertion description "[For this purpose, we have investigated the menin gene mutations in 21 sporadic parathyroid adenomas, 2 parathyroid carcinomas, 4 sporadic insulinomas, and 1 malignant VIP (vasoactive intestinal polypeptide)oma with WDHA (watery diarrhea, hypokalemia, and achlorhydria) syndrome, using PCR-single strand conformation polymorphism analysis and DNA sequencing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP434546.RA7wYT2Th6ApSaL0d6sovUZslWnc2npTdYOVEtPQEudyI130_provenance.
- NP434546.RA7wYT2Th6ApSaL0d6sovUZslWnc2npTdYOVEtPQEudyI130_assertion evidence source_evidence_literature NP434546.RA7wYT2Th6ApSaL0d6sovUZslWnc2npTdYOVEtPQEudyI130_provenance.
- NP434546.RA7wYT2Th6ApSaL0d6sovUZslWnc2npTdYOVEtPQEudyI130_assertion SIO_000772 9564891 NP434546.RA7wYT2Th6ApSaL0d6sovUZslWnc2npTdYOVEtPQEudyI130_provenance.
- NP434546.RA7wYT2Th6ApSaL0d6sovUZslWnc2npTdYOVEtPQEudyI130_assertion wasDerivedFrom befree-20140225 NP434546.RA7wYT2Th6ApSaL0d6sovUZslWnc2npTdYOVEtPQEudyI130_provenance.
- NP434546.RA7wYT2Th6ApSaL0d6sovUZslWnc2npTdYOVEtPQEudyI130_assertion wasGeneratedBy ECO_0000203 NP434546.RA7wYT2Th6ApSaL0d6sovUZslWnc2npTdYOVEtPQEudyI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP434546.RA7wYT2Th6ApSaL0d6sovUZslWnc2npTdYOVEtPQEudyI130_provenance.