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- NP262383.RA14x-zTG8NuIb-1nv65xp1cmYdW0an5bi7het1YaCL7Q130_assertion type Assertion NP262383.RA14x-zTG8NuIb-1nv65xp1cmYdW0an5bi7het1YaCL7Q130_head.
- NP262383.RA14x-zTG8NuIb-1nv65xp1cmYdW0an5bi7het1YaCL7Q130_assertion wasGeneratedBy ECO_0000203 NP262383.RA14x-zTG8NuIb-1nv65xp1cmYdW0an5bi7het1YaCL7Q130_provenance.
- NP262383.RA14x-zTG8NuIb-1nv65xp1cmYdW0an5bi7het1YaCL7Q130_assertion wasDerivedFrom befree-20140225 NP262383.RA14x-zTG8NuIb-1nv65xp1cmYdW0an5bi7het1YaCL7Q130_provenance.
- NP262383.RA14x-zTG8NuIb-1nv65xp1cmYdW0an5bi7het1YaCL7Q130_assertion SIO_000772 18363760 NP262383.RA14x-zTG8NuIb-1nv65xp1cmYdW0an5bi7het1YaCL7Q130_provenance.
- NP262383.RA14x-zTG8NuIb-1nv65xp1cmYdW0an5bi7het1YaCL7Q130_assertion evidence source_evidence_literature NP262383.RA14x-zTG8NuIb-1nv65xp1cmYdW0an5bi7het1YaCL7Q130_provenance.
- NP262383.RA14x-zTG8NuIb-1nv65xp1cmYdW0an5bi7het1YaCL7Q130_assertion description "[Recently a rare form of hereditary vascular malformation termed capillary malformation-arteriovenous malformation (CM-AVM) was shown to be caused by heterozygous mutations in RASA1, encoding RAS p21 protein activator 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262383.RA14x-zTG8NuIb-1nv65xp1cmYdW0an5bi7het1YaCL7Q130_provenance.