Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP852946.RAKleQH0bjHBUqS-hOxZ6dEHSxi-dGjv0sgzrr7aaq7JA130_assertion> ?p ?o ?g. }
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- NP852946.RAKleQH0bjHBUqS-hOxZ6dEHSxi-dGjv0sgzrr7aaq7JA130_assertion type Assertion NP852946.RAKleQH0bjHBUqS-hOxZ6dEHSxi-dGjv0sgzrr7aaq7JA130_head.
- NP852946.RAKleQH0bjHBUqS-hOxZ6dEHSxi-dGjv0sgzrr7aaq7JA130_assertion description "[Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant and age-dependent vascular disorder originated by mutations in Endoglin (ENG) or activin receptor-like kinase-1 (ALK1, ACVRL1) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP852946.RAKleQH0bjHBUqS-hOxZ6dEHSxi-dGjv0sgzrr7aaq7JA130_provenance.
- NP852946.RAKleQH0bjHBUqS-hOxZ6dEHSxi-dGjv0sgzrr7aaq7JA130_assertion evidence source_evidence_literature NP852946.RAKleQH0bjHBUqS-hOxZ6dEHSxi-dGjv0sgzrr7aaq7JA130_provenance.
- NP852946.RAKleQH0bjHBUqS-hOxZ6dEHSxi-dGjv0sgzrr7aaq7JA130_assertion SIO_000772 16470589 NP852946.RAKleQH0bjHBUqS-hOxZ6dEHSxi-dGjv0sgzrr7aaq7JA130_provenance.
- NP852946.RAKleQH0bjHBUqS-hOxZ6dEHSxi-dGjv0sgzrr7aaq7JA130_assertion wasDerivedFrom befree-20140225 NP852946.RAKleQH0bjHBUqS-hOxZ6dEHSxi-dGjv0sgzrr7aaq7JA130_provenance.
- NP852946.RAKleQH0bjHBUqS-hOxZ6dEHSxi-dGjv0sgzrr7aaq7JA130_assertion wasGeneratedBy ECO_0000203 NP852946.RAKleQH0bjHBUqS-hOxZ6dEHSxi-dGjv0sgzrr7aaq7JA130_provenance.