Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1249641.RAUDmIN4Bri9hmVMW3KhHwp3NmWKzEoQP9YniE_CrQ_Rs130_assertion> ?p ?o ?g. }
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- NP1249641.RAUDmIN4Bri9hmVMW3KhHwp3NmWKzEoQP9YniE_CrQ_Rs130_assertion type Assertion NP1249641.RAUDmIN4Bri9hmVMW3KhHwp3NmWKzEoQP9YniE_CrQ_Rs130_head.
- 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.
- NP1249641.RAUDmIN4Bri9hmVMW3KhHwp3NmWKzEoQP9YniE_CrQ_Rs130_assertion evidence source_evidence_literature NP1249641.RAUDmIN4Bri9hmVMW3KhHwp3NmWKzEoQP9YniE_CrQ_Rs130_provenance.
- NP1249641.RAUDmIN4Bri9hmVMW3KhHwp3NmWKzEoQP9YniE_CrQ_Rs130_assertion SIO_000772 25525273 NP1249641.RAUDmIN4Bri9hmVMW3KhHwp3NmWKzEoQP9YniE_CrQ_Rs130_provenance.
- NP1249641.RAUDmIN4Bri9hmVMW3KhHwp3NmWKzEoQP9YniE_CrQ_Rs130_assertion wasDerivedFrom befree-2016 NP1249641.RAUDmIN4Bri9hmVMW3KhHwp3NmWKzEoQP9YniE_CrQ_Rs130_provenance.
- NP1249641.RAUDmIN4Bri9hmVMW3KhHwp3NmWKzEoQP9YniE_CrQ_Rs130_assertion wasGeneratedBy ECO_0000203 NP1249641.RAUDmIN4Bri9hmVMW3KhHwp3NmWKzEoQP9YniE_CrQ_Rs130_provenance.