Matches in Nanopublications for { ?s ?p "[Individuals with germline mutations of the SHH receptor gene PTCH are at high risk of developmental anomalies and of basal-cell carcinomas, medulloblastomas and other cancers (a pattern consistent with nevoid basal-cell carcinoma syndrome, NBCCS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP288008.RABpEFgTilA9M7KTmi7C80PVUho54vrQ7dq_hdd6IiB5E130_assertion description "[Individuals with germline mutations of the SHH receptor gene PTCH are at high risk of developmental anomalies and of basal-cell carcinomas, medulloblastomas and other cancers (a pattern consistent with nevoid basal-cell carcinoma syndrome, NBCCS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP288008.RABpEFgTilA9M7KTmi7C80PVUho54vrQ7dq_hdd6IiB5E130_provenance.
- assertion description "[Individuals with germline mutations of the SHH receptor gene PTCH are at high risk of developmental anomalies and of basal-cell carcinomas, medulloblastomas and other cancers (a pattern consistent with nevoid basal-cell carcinoma syndrome, NBCCS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Individuals with germline mutations of the SHH receptor gene PTCH are at high risk of developmental anomalies and of basal-cell carcinomas, medulloblastomas and other cancers (a pattern consistent with nevoid basal-cell carcinoma syndrome, NBCCS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.