Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Almost one fourth of patients with apparently sporadic pheochromocytoma may be carriers of mutations; routine analysis for mutations of RET, VHL, SDHD, and SDHB is indicated to identify pheochromocytoma-associated syndromes that would otherwise be missed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP52082.RAqUpSq1NZx452NgyJ02GP1j72b8R847fOUYE2KSucIb8130_assertion description "[Almost one fourth of patients with apparently sporadic pheochromocytoma may be carriers of mutations; routine analysis for mutations of RET, VHL, SDHD, and SDHB is indicated to identify pheochromocytoma-associated syndromes that would otherwise be missed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52082.RAqUpSq1NZx452NgyJ02GP1j72b8R847fOUYE2KSucIb8130_provenance.
• NP52313.RAlNvxHVRIlyUrkX-tGXVqxgZloa4wAA6WpxTCrtO2beE130_assertion description "[Almost one fourth of patients with apparently sporadic pheochromocytoma may be carriers of mutations; routine analysis for mutations of RET, VHL, SDHD, and SDHB is indicated to identify pheochromocytoma-associated syndromes that would otherwise be missed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52313.RAlNvxHVRIlyUrkX-tGXVqxgZloa4wAA6WpxTCrtO2beE130_provenance.
• NP59235.RA54CBDUH5riF9gYnUcvMkpIgp769pPYKGYABnmPuxii0130_assertion description "[Almost one fourth of patients with apparently sporadic pheochromocytoma may be carriers of mutations; routine analysis for mutations of RET, VHL, SDHD, and SDHB is indicated to identify pheochromocytoma-associated syndromes that would otherwise be missed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59235.RA54CBDUH5riF9gYnUcvMkpIgp769pPYKGYABnmPuxii0130_provenance.
• NP52085.RAEPpLI-70kbTfVsWCkAot5YzDIyBaHkLuaeK-8GErNOw130_assertion description "[Almost one fourth of patients with apparently sporadic pheochromocytoma may be carriers of mutations; routine analysis for mutations of RET, VHL, SDHD, and SDHB is indicated to identify pheochromocytoma-associated syndromes that would otherwise be missed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52085.RAEPpLI-70kbTfVsWCkAot5YzDIyBaHkLuaeK-8GErNOw130_provenance.
• NP28488.RAcGuMm7TqXsOd8lwQv7zW9aFUGNMJxSIdKR_zZ35l9qA130_assertion description "[Almost one fourth of patients with apparently sporadic pheochromocytoma may be carriers of mutations; routine analysis for mutations of RET, VHL, SDHD, and SDHB is indicated to identify pheochromocytoma-associated syndromes that would otherwise be missed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP28488.RAcGuMm7TqXsOd8lwQv7zW9aFUGNMJxSIdKR_zZ35l9qA130_provenance.
• assertion description "[Almost one fourth of patients with apparently sporadic pheochromocytoma may be carriers of mutations; routine analysis for mutations of RET, VHL, SDHD, and SDHB is indicated to identify pheochromocytoma-associated syndromes that would otherwise be missed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Almost one fourth of patients with apparently sporadic pheochromocytoma may be carriers of mutations; routine analysis for mutations of RET, VHL, SDHD, and SDHB is indicated to identify pheochromocytoma-associated syndromes that would otherwise be missed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP354313.RAc-AcHbrkiewxlTvsg5fdWSePEJikOgaarUttCG7RvdU130_assertion description "[Almost one fourth of patients with apparently sporadic pheochromocytoma may be carriers of mutations; routine analysis for mutations of RET, VHL, SDHD, and SDHB is indicated to identify pheochromocytoma-associated syndromes that would otherwise be missed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP354313.RAc-AcHbrkiewxlTvsg5fdWSePEJikOgaarUttCG7RvdU130_provenance.
• NP2026.RAhztEJRlHrUDiRpuppQiaollGzGaplN0pLy2fcZ1Jtig130_assertion description "[Almost one fourth of patients with apparently sporadic pheochromocytoma may be carriers of mutations; routine analysis for mutations of RET, VHL, SDHD, and SDHB is indicated to identify pheochromocytoma-associated syndromes that would otherwise be missed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2026.RAhztEJRlHrUDiRpuppQiaollGzGaplN0pLy2fcZ1Jtig130_provenance.
• NP2029.RAuRwjUUeDqtpSX1DI210N_VgmMhqfZjhjQR7aYKEXT8c130_assertion description "[Almost one fourth of patients with apparently sporadic pheochromocytoma may be carriers of mutations; routine analysis for mutations of RET, VHL, SDHD, and SDHB is indicated to identify pheochromocytoma-associated syndromes that would otherwise be missed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2029.RAuRwjUUeDqtpSX1DI210N_VgmMhqfZjhjQR7aYKEXT8c130_provenance.
• NP2027.RA77mVIJG2cIPPo6lb5fI7ElF_dEv_r7qt964ytwQJ1QU130_assertion description "[Almost one fourth of patients with apparently sporadic pheochromocytoma may be carriers of mutations; routine analysis for mutations of RET, VHL, SDHD, and SDHB is indicated to identify pheochromocytoma-associated syndromes that would otherwise be missed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2027.RA77mVIJG2cIPPo6lb5fI7ElF_dEv_r7qt964ytwQJ1QU130_provenance.
• NP11973.RAzEwqDl3F69-A9ielsl9fjDdv0d10XvvX2gvIKeLv_bk130_assertion description "[Almost one fourth of patients with apparently sporadic pheochromocytoma may be carriers of mutations; routine analysis for mutations of RET, VHL, SDHD, and SDHB is indicated to identify pheochromocytoma-associated syndromes that would otherwise be missed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP11973.RAzEwqDl3F69-A9ielsl9fjDdv0d10XvvX2gvIKeLv_bk130_provenance.