Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP829071.RAKioMXlVzdrH0G1OAE0kj3_MGMf7WoyqPueetF2oV7do130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP829071.RAKioMXlVzdrH0G1OAE0kj3_MGMf7WoyqPueetF2oV7do130_assertion type Assertion NP829071.RAKioMXlVzdrH0G1OAE0kj3_MGMf7WoyqPueetF2oV7do130_head.
- NP829071.RAKioMXlVzdrH0G1OAE0kj3_MGMf7WoyqPueetF2oV7do130_assertion wasGeneratedBy ECO_0000203 NP829071.RAKioMXlVzdrH0G1OAE0kj3_MGMf7WoyqPueetF2oV7do130_provenance.
- NP829071.RAKioMXlVzdrH0G1OAE0kj3_MGMf7WoyqPueetF2oV7do130_assertion wasDerivedFrom befree-20140225 NP829071.RAKioMXlVzdrH0G1OAE0kj3_MGMf7WoyqPueetF2oV7do130_provenance.
- NP829071.RAKioMXlVzdrH0G1OAE0kj3_MGMf7WoyqPueetF2oV7do130_assertion SIO_000772 18363760 NP829071.RAKioMXlVzdrH0G1OAE0kj3_MGMf7WoyqPueetF2oV7do130_provenance.
- NP829071.RAKioMXlVzdrH0G1OAE0kj3_MGMf7WoyqPueetF2oV7do130_assertion evidence source_evidence_literature NP829071.RAKioMXlVzdrH0G1OAE0kj3_MGMf7WoyqPueetF2oV7do130_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.