Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP655892.RAl7S2pLH8jTBJ3TJ9Pf_aQdeD5jpU959J4Yyg6HeDX7Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP655892.RAl7S2pLH8jTBJ3TJ9Pf_aQdeD5jpU959J4Yyg6HeDX7Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP655892.RAl7S2pLH8jTBJ3TJ9Pf_aQdeD5jpU959J4Yyg6HeDX7Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP655892.RAl7S2pLH8jTBJ3TJ9Pf_aQdeD5jpU959J4Yyg6HeDX7Y130_provenance.
- NP655892.RAl7S2pLH8jTBJ3TJ9Pf_aQdeD5jpU959J4Yyg6HeDX7Y130_assertion description "[This paper briefly reviews the clinically most important new knowledge on sporadic and hereditary forms of parathyroid hormone-dependent hypercalcemic disorders, with special emphasis on familial syndromes such as multiple endocrine neoplasia type 1 and type 2A, hyperparathyroidism-jaw tumor syndrome, familial isolated hyperparathyroidism, familial hypocalciuric hypercalcemia and neonatal severe primary hyperparathyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP655892.RAl7S2pLH8jTBJ3TJ9Pf_aQdeD5jpU959J4Yyg6HeDX7Y130_provenance.
- NP655892.RAl7S2pLH8jTBJ3TJ9Pf_aQdeD5jpU959J4Yyg6HeDX7Y130_assertion evidence source_evidence_literature NP655892.RAl7S2pLH8jTBJ3TJ9Pf_aQdeD5jpU959J4Yyg6HeDX7Y130_provenance.
- NP655892.RAl7S2pLH8jTBJ3TJ9Pf_aQdeD5jpU959J4Yyg6HeDX7Y130_assertion SIO_000772 19562279 NP655892.RAl7S2pLH8jTBJ3TJ9Pf_aQdeD5jpU959J4Yyg6HeDX7Y130_provenance.
- NP655892.RAl7S2pLH8jTBJ3TJ9Pf_aQdeD5jpU959J4Yyg6HeDX7Y130_assertion wasDerivedFrom befree-20150227 NP655892.RAl7S2pLH8jTBJ3TJ9Pf_aQdeD5jpU959J4Yyg6HeDX7Y130_provenance.
- NP655892.RAl7S2pLH8jTBJ3TJ9Pf_aQdeD5jpU959J4Yyg6HeDX7Y130_assertion wasGeneratedBy ECO_0000203 NP655892.RAl7S2pLH8jTBJ3TJ9Pf_aQdeD5jpU959J4Yyg6HeDX7Y130_provenance.
- befree-20150227 importedOn "2015-02-27" NP655892.RAl7S2pLH8jTBJ3TJ9Pf_aQdeD5jpU959J4Yyg6HeDX7Y130_provenance.