Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[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."@en ?g. }

• NP807050.RABONkKkM7Yn-ifghP7nYUIwxPeZbLuwqeWWcPNRm2Si8130_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." NP807050.RABONkKkM7Yn-ifghP7nYUIwxPeZbLuwqeWWcPNRm2Si8130_provenance.
• NP631072.RAOO5awtAXMBvWOvgGdp-6qsvDJkPifDareclH_qvGxag130_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." NP631072.RAOO5awtAXMBvWOvgGdp-6qsvDJkPifDareclH_qvGxag130_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.
• NP662227.RACDD-DVcBFDNdR4OUhd43dafZ0bQjs7Ptw9v-IE6TFG0130_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." NP662227.RACDD-DVcBFDNdR4OUhd43dafZ0bQjs7Ptw9v-IE6TFG0130_provenance.
• NP829071.RAKioMXlVzdrH0G1OAE0kj3_MGMf7WoyqPueetF2oV7do130_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." NP829071.RAKioMXlVzdrH0G1OAE0kj3_MGMf7WoyqPueetF2oV7do130_provenance.
• NP807077.RAw9tA8ChzpxNKI2yrA8F3ixK9R6xa_FUnjDF3YswpWDE130_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." NP807077.RAw9tA8ChzpxNKI2yrA8F3ixK9R6xa_FUnjDF3YswpWDE130_provenance.
• NP666534.RASi2Qk7Ia0J8yOxgnx-WOOuRbRg8Js-M3eDVHIjQj4NE130_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." NP666534.RASi2Qk7Ia0J8yOxgnx-WOOuRbRg8Js-M3eDVHIjQj4NE130_provenance.
• NP662226.RA9UssshVtnJh5mYwBuxiHQ6oM0qAOqIUqJR0-yVCqcvY130_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." NP662226.RA9UssshVtnJh5mYwBuxiHQ6oM0qAOqIUqJR0-yVCqcvY130_provenance.
• NP662230.RASUe0NPgqdSihtHZk3jgToqxBa-AZQCODWmnLPPMp-L4130_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." NP662230.RASUe0NPgqdSihtHZk3jgToqxBa-AZQCODWmnLPPMp-L4130_provenance.
• 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." provenance.
• 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." provenance.
• 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." provenance.
• NP666458.RAv6_hR2i4XwvIyIjvKeuJ9EU_uG1lectoq1SJ9S9xKZU130_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." NP666458.RAv6_hR2i4XwvIyIjvKeuJ9EU_uG1lectoq1SJ9S9xKZU130_provenance.
• NP666544.RAjk8maFzKqkCZeVQP0Wu66_MKsCk9rDqkMgv8jrJAxys130_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." NP666544.RAjk8maFzKqkCZeVQP0Wu66_MKsCk9rDqkMgv8jrJAxys130_provenance.
• NP662231.RAKBWjWxIUiissi7d7d-FqAoau_Zz1TUWrmaXf7dBKJhc130_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." NP662231.RAKBWjWxIUiissi7d7d-FqAoau_Zz1TUWrmaXf7dBKJhc130_provenance.
• NP662233.RAMsC39SjC-FRx9cosSaP6oJvIrtiF7I2ztCfkbAtbJcc130_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." NP662233.RAMsC39SjC-FRx9cosSaP6oJvIrtiF7I2ztCfkbAtbJcc130_provenance.
• NP662235.RAKIojRT81WpWSYaeJCd5NguZs8-nulEO4Ynb9vneinAw130_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." NP662235.RAKIojRT81WpWSYaeJCd5NguZs8-nulEO4Ynb9vneinAw130_provenance.
• NP807070.RAsXDpQ1qWbVXA9uODSTpW4TEKC55_-Fc84ZQaVu2g2dY130_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." NP807070.RAsXDpQ1qWbVXA9uODSTpW4TEKC55_-Fc84ZQaVu2g2dY130_provenance.