Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP662235.RAKIojRT81WpWSYaeJCd5NguZs8-nulEO4Ynb9vneinAw130_assertion> ?p ?o ?g. }
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- NP662235.RAKIojRT81WpWSYaeJCd5NguZs8-nulEO4Ynb9vneinAw130_assertion type Assertion NP662235.RAKIojRT81WpWSYaeJCd5NguZs8-nulEO4Ynb9vneinAw130_head.
- NP662235.RAKIojRT81WpWSYaeJCd5NguZs8-nulEO4Ynb9vneinAw130_assertion wasGeneratedBy ECO_0000203 NP662235.RAKIojRT81WpWSYaeJCd5NguZs8-nulEO4Ynb9vneinAw130_provenance.
- NP662235.RAKIojRT81WpWSYaeJCd5NguZs8-nulEO4Ynb9vneinAw130_assertion wasDerivedFrom befree-2016 NP662235.RAKIojRT81WpWSYaeJCd5NguZs8-nulEO4Ynb9vneinAw130_provenance.
- NP662235.RAKIojRT81WpWSYaeJCd5NguZs8-nulEO4Ynb9vneinAw130_assertion SIO_000772 18363760 NP662235.RAKIojRT81WpWSYaeJCd5NguZs8-nulEO4Ynb9vneinAw130_provenance.
- NP662235.RAKIojRT81WpWSYaeJCd5NguZs8-nulEO4Ynb9vneinAw130_assertion evidence source_evidence_literature NP662235.RAKIojRT81WpWSYaeJCd5NguZs8-nulEO4Ynb9vneinAw130_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.