Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP277524.RAP_w7Nm7--rH_zhXQP5TaQxQbTkM6q-rqoxEt6dPNIzo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP277524.RAP_w7Nm7--rH_zhXQP5TaQxQbTkM6q-rqoxEt6dPNIzo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP277524.RAP_w7Nm7--rH_zhXQP5TaQxQbTkM6q-rqoxEt6dPNIzo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP277524.RAP_w7Nm7--rH_zhXQP5TaQxQbTkM6q-rqoxEt6dPNIzo130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP277524.RAP_w7Nm7--rH_zhXQP5TaQxQbTkM6q-rqoxEt6dPNIzo130_provenance.