Matches in Nanopublications for { ?s ?p "[Hyperparathyroidism-jaw tumor syndrome (HPT-JT) is a rare autosomal disease caused by inactivating germ-line mutations of HRPT2 gene, with subsequent loss of Parafibromin expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP212253.RAAbhvcnkuxbrzwAAsjRkJD-FcqzIAxl4E6JhgkyrCn-A130_assertion description "[Hyperparathyroidism-jaw tumor syndrome (HPT-JT) is a rare autosomal disease caused by inactivating germ-line mutations of HRPT2 gene, with subsequent loss of Parafibromin expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP212253.RAAbhvcnkuxbrzwAAsjRkJD-FcqzIAxl4E6JhgkyrCn-A130_provenance.
- assertion description "[Hyperparathyroidism-jaw tumor syndrome (HPT-JT) is a rare autosomal disease caused by inactivating germ-line mutations of HRPT2 gene, with subsequent loss of Parafibromin expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP745513.RAPnsAvr0QPo7TtOJ-wKv_-wgOMgL9kps1sE1hk41slw4130_assertion description "[Hyperparathyroidism-jaw tumor syndrome (HPT-JT) is a rare autosomal disease caused by inactivating germ-line mutations of HRPT2 gene, with subsequent loss of Parafibromin expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP745513.RAPnsAvr0QPo7TtOJ-wKv_-wgOMgL9kps1sE1hk41slw4130_provenance.