Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP277524.RAP_w7Nm7--rH_zhXQP5TaQxQbTkM6q-rqoxEt6dPNIzo130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP277524.RAP_w7Nm7--rH_zhXQP5TaQxQbTkM6q-rqoxEt6dPNIzo130_assertion type Assertion NP277524.RAP_w7Nm7--rH_zhXQP5TaQxQbTkM6q-rqoxEt6dPNIzo130_head.
- NP277524.RAP_w7Nm7--rH_zhXQP5TaQxQbTkM6q-rqoxEt6dPNIzo130_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." NP277524.RAP_w7Nm7--rH_zhXQP5TaQxQbTkM6q-rqoxEt6dPNIzo130_provenance.
- NP277524.RAP_w7Nm7--rH_zhXQP5TaQxQbTkM6q-rqoxEt6dPNIzo130_assertion evidence source_evidence_literature NP277524.RAP_w7Nm7--rH_zhXQP5TaQxQbTkM6q-rqoxEt6dPNIzo130_provenance.
- NP277524.RAP_w7Nm7--rH_zhXQP5TaQxQbTkM6q-rqoxEt6dPNIzo130_assertion SIO_000772 16179574 NP277524.RAP_w7Nm7--rH_zhXQP5TaQxQbTkM6q-rqoxEt6dPNIzo130_provenance.
- NP277524.RAP_w7Nm7--rH_zhXQP5TaQxQbTkM6q-rqoxEt6dPNIzo130_assertion wasDerivedFrom befree-20140225 NP277524.RAP_w7Nm7--rH_zhXQP5TaQxQbTkM6q-rqoxEt6dPNIzo130_provenance.
- NP277524.RAP_w7Nm7--rH_zhXQP5TaQxQbTkM6q-rqoxEt6dPNIzo130_assertion wasGeneratedBy ECO_0000203 NP277524.RAP_w7Nm7--rH_zhXQP5TaQxQbTkM6q-rqoxEt6dPNIzo130_provenance.