Matches in Nanopublications for { ?s ?p "[We report here that a subset of children with medulloblastoma carry germline and somatic mutations in SUFU (encoding the human suppressor of fused) of the SHH pathway, accompanied by loss of heterozygosity of the wildtype allele.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP542048.RAepcXiTMWPkj4XJ146oj7xGpCdt3O84BxxTAaLnMl6b8130_assertion description "[We report here that a subset of children with medulloblastoma carry germline and somatic mutations in SUFU (encoding the human suppressor of fused) of the SHH pathway, accompanied by loss of heterozygosity of the wildtype allele.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP542048.RAepcXiTMWPkj4XJ146oj7xGpCdt3O84BxxTAaLnMl6b8130_provenance.
- assertion description "[We report here that a subset of children with medulloblastoma carry germline and somatic mutations in SUFU (encoding the human suppressor of fused) of the SHH pathway, accompanied by loss of heterozygosity of the wildtype allele.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP358016.RArXgk-TnEaW7g0HhQX9fxTnU2gcEesc5IU2IpaeyDUqA130_assertion description "[We report here that a subset of children with medulloblastoma carry germline and somatic mutations in SUFU (encoding the human suppressor of fused) of the SHH pathway, accompanied by loss of heterozygosity of the wildtype allele.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP358016.RArXgk-TnEaW7g0HhQX9fxTnU2gcEesc5IU2IpaeyDUqA130_provenance.