Matches in Nanopublications for { ?s ?p "[Germline mutations in the SMARCB1 gene cause familial schwannomatosis, a condition characterized by the presence of multiple schwannomas, although mutations in SMARCB1 have also been associated with rhadboid tumor predisposition syndrome 1 (RTPS1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP685136.RAr88LJ4iZKeMkH5T-ZHgmatbK_VR_1ZRHJ52TQRHyN5o130_assertion description "[Germline mutations in the SMARCB1 gene cause familial schwannomatosis, a condition characterized by the presence of multiple schwannomas, although mutations in SMARCB1 have also been associated with rhadboid tumor predisposition syndrome 1 (RTPS1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP685136.RAr88LJ4iZKeMkH5T-ZHgmatbK_VR_1ZRHJ52TQRHyN5o130_provenance.
- NP994635.RAqI9Vi-LwRJKj1-wUgSzphAl1s1KwAcRYI0IIYduaT_0130_assertion description "[Germline mutations in the SMARCB1 gene cause familial schwannomatosis, a condition characterized by the presence of multiple schwannomas, although mutations in SMARCB1 have also been associated with rhadboid tumor predisposition syndrome 1 (RTPS1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP994635.RAqI9Vi-LwRJKj1-wUgSzphAl1s1KwAcRYI0IIYduaT_0130_provenance.
- NP703151.RA68fyjMLVj7mWZETky3vQYgWB3pjOL3efh1vHaV5HGxA130_assertion description "[Germline mutations in the SMARCB1 gene cause familial schwannomatosis, a condition characterized by the presence of multiple schwannomas, although mutations in SMARCB1 have also been associated with rhadboid tumor predisposition syndrome 1 (RTPS1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP703151.RA68fyjMLVj7mWZETky3vQYgWB3pjOL3efh1vHaV5HGxA130_provenance.