Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP656277.RA9ibS5Nm-I_T8V7VkZkuNWNsXPaTDftR0UPoy8Em-ho0130_assertion> ?p ?o ?g. }
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- NP656277.RA9ibS5Nm-I_T8V7VkZkuNWNsXPaTDftR0UPoy8Em-ho0130_assertion type Assertion NP656277.RA9ibS5Nm-I_T8V7VkZkuNWNsXPaTDftR0UPoy8Em-ho0130_head.
- NP656277.RA9ibS5Nm-I_T8V7VkZkuNWNsXPaTDftR0UPoy8Em-ho0130_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." NP656277.RA9ibS5Nm-I_T8V7VkZkuNWNsXPaTDftR0UPoy8Em-ho0130_provenance.
- NP656277.RA9ibS5Nm-I_T8V7VkZkuNWNsXPaTDftR0UPoy8Em-ho0130_assertion evidence source_evidence_literature NP656277.RA9ibS5Nm-I_T8V7VkZkuNWNsXPaTDftR0UPoy8Em-ho0130_provenance.
- NP656277.RA9ibS5Nm-I_T8V7VkZkuNWNsXPaTDftR0UPoy8Em-ho0130_assertion SIO_000772 19562279 NP656277.RA9ibS5Nm-I_T8V7VkZkuNWNsXPaTDftR0UPoy8Em-ho0130_provenance.
- NP656277.RA9ibS5Nm-I_T8V7VkZkuNWNsXPaTDftR0UPoy8Em-ho0130_assertion wasDerivedFrom befree-20150227 NP656277.RA9ibS5Nm-I_T8V7VkZkuNWNsXPaTDftR0UPoy8Em-ho0130_provenance.
- NP656277.RA9ibS5Nm-I_T8V7VkZkuNWNsXPaTDftR0UPoy8Em-ho0130_assertion wasGeneratedBy ECO_0000203 NP656277.RA9ibS5Nm-I_T8V7VkZkuNWNsXPaTDftR0UPoy8Em-ho0130_provenance.