Matches in Nanopublications for { ?s ?p "[Mutations in both alleles of the tumour suppressor gene coding for merlin/schwannomin, an ERM family protein, cause the hereditary disease neurofibromatosis type 2 (NF2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP221768.RAeOkAYeyHyQShDmlsur_95xSnE7FjHNkmz1GYbHnPTKs130_assertion description "[Mutations in both alleles of the tumour suppressor gene coding for merlin/schwannomin, an ERM family protein, cause the hereditary disease neurofibromatosis type 2 (NF2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221768.RAeOkAYeyHyQShDmlsur_95xSnE7FjHNkmz1GYbHnPTKs130_provenance.
- NP648522.RAh_FR2xh5-bvJMDkk936YP0QxT6iXGGQG9KtzePrMWRY130_assertion description "[Mutations in both alleles of the tumour suppressor gene coding for merlin/schwannomin, an ERM family protein, cause the hereditary disease neurofibromatosis type 2 (NF2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP648522.RAh_FR2xh5-bvJMDkk936YP0QxT6iXGGQG9KtzePrMWRY130_provenance.
- NP599592.RAcO2bzGVxcukBBvaexX-bi2jx8Lm9H3Jj2sF6-n-bzYw130_assertion description "[Mutations in both alleles of the tumour suppressor gene coding for merlin/schwannomin, an ERM family protein, cause the hereditary disease neurofibromatosis type 2 (NF2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP599592.RAcO2bzGVxcukBBvaexX-bi2jx8Lm9H3Jj2sF6-n-bzYw130_provenance.
- NP204296.RAluelHzN77wpOg8S5NVNLN3pjAejMfFjREtYlWIx8b3o130_assertion description "[Mutations in both alleles of the tumour suppressor gene coding for merlin/schwannomin, an ERM family protein, cause the hereditary disease neurofibromatosis type 2 (NF2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP204296.RAluelHzN77wpOg8S5NVNLN3pjAejMfFjREtYlWIx8b3o130_provenance.
- NP917081.RAhnTiakAF2i0AjTYJGyuH2PcNgw302OfUcKMmAMvA7Hk130_assertion description "[Mutations in both alleles of the tumour suppressor gene coding for merlin/schwannomin, an ERM family protein, cause the hereditary disease neurofibromatosis type 2 (NF2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP917081.RAhnTiakAF2i0AjTYJGyuH2PcNgw302OfUcKMmAMvA7Hk130_provenance.