Matches in Nanopublications for { ?s ?p "[Familial cerebral cavernous malformations (CCMs) are predominantly neurovascular lesions and are associated with mutations within the KRIT1, CCM2, and PDCD10 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Familial cerebral cavernous malformations (CCMs) are predominantly neurovascular lesions and are associated with mutations within the KRIT1, CCM2, and PDCD10 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Familial cerebral cavernous malformations (CCMs) are predominantly neurovascular lesions and are associated with mutations within the KRIT1, CCM2, and PDCD10 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1249641.RAUDmIN4Bri9hmVMW3KhHwp3NmWKzEoQP9YniE_CrQ_Rs130_assertion description "[Familial cerebral cavernous malformations (CCMs) are predominantly neurovascular lesions and are associated with mutations within the KRIT1, CCM2, and PDCD10 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1249641.RAUDmIN4Bri9hmVMW3KhHwp3NmWKzEoQP9YniE_CrQ_Rs130_provenance.
- NP1249640.RAAIVjKKDDwYJVrJgWcU3bHEEpZLwyoXAqydAfT5hEQEQ130_assertion description "[Familial cerebral cavernous malformations (CCMs) are predominantly neurovascular lesions and are associated with mutations within the KRIT1, CCM2, and PDCD10 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1249640.RAAIVjKKDDwYJVrJgWcU3bHEEpZLwyoXAqydAfT5hEQEQ130_provenance.