Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP489211.RAdl8VLTuznL3Vw-avBWQve3xn3tzHyGQ3bkVUdSxO0Kc130_assertion> ?p ?o ?g. }
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- NP489211.RAdl8VLTuznL3Vw-avBWQve3xn3tzHyGQ3bkVUdSxO0Kc130_assertion type Assertion NP489211.RAdl8VLTuznL3Vw-avBWQve3xn3tzHyGQ3bkVUdSxO0Kc130_head.
- NP489211.RAdl8VLTuznL3Vw-avBWQve3xn3tzHyGQ3bkVUdSxO0Kc130_assertion description "[Mutations in endoglin (ENG) and activin-like kinase (ALK1) cause hereditary hemorrhagic telangiectasias, disorders characterized by pulmonary and brain arteriovenous malformations (BAVMs).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP489211.RAdl8VLTuznL3Vw-avBWQve3xn3tzHyGQ3bkVUdSxO0Kc130_provenance.
- NP489211.RAdl8VLTuznL3Vw-avBWQve3xn3tzHyGQ3bkVUdSxO0Kc130_assertion evidence source_evidence_literature NP489211.RAdl8VLTuznL3Vw-avBWQve3xn3tzHyGQ3bkVUdSxO0Kc130_provenance.
- NP489211.RAdl8VLTuznL3Vw-avBWQve3xn3tzHyGQ3bkVUdSxO0Kc130_assertion SIO_000772 16179574 NP489211.RAdl8VLTuznL3Vw-avBWQve3xn3tzHyGQ3bkVUdSxO0Kc130_provenance.
- NP489211.RAdl8VLTuznL3Vw-avBWQve3xn3tzHyGQ3bkVUdSxO0Kc130_assertion wasDerivedFrom befree-20140225 NP489211.RAdl8VLTuznL3Vw-avBWQve3xn3tzHyGQ3bkVUdSxO0Kc130_provenance.
- NP489211.RAdl8VLTuznL3Vw-avBWQve3xn3tzHyGQ3bkVUdSxO0Kc130_assertion wasGeneratedBy ECO_0000203 NP489211.RAdl8VLTuznL3Vw-avBWQve3xn3tzHyGQ3bkVUdSxO0Kc130_provenance.