Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP374933.RAbn0b-Le2ZCbecl0oPFT4I4tXZ9sG6ZWTaj8ohkw1V8M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP374933.RAbn0b-Le2ZCbecl0oPFT4I4tXZ9sG6ZWTaj8ohkw1V8M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP374933.RAbn0b-Le2ZCbecl0oPFT4I4tXZ9sG6ZWTaj8ohkw1V8M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP374933.RAbn0b-Le2ZCbecl0oPFT4I4tXZ9sG6ZWTaj8ohkw1V8M130_provenance.
- NP374933.RAbn0b-Le2ZCbecl0oPFT4I4tXZ9sG6ZWTaj8ohkw1V8M130_assertion description "[Defective TGF-beta signaling in endothelial cells attributable to mutations in endoglin or the type I receptor ALK-1 leads to hereditary hemorrhagic telangiectasia, whereas defective BMP signaling attributable to mutations in the BMP receptor II has been associated with development of primary pulmonary hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP374933.RAbn0b-Le2ZCbecl0oPFT4I4tXZ9sG6ZWTaj8ohkw1V8M130_provenance.
- NP374933.RAbn0b-Le2ZCbecl0oPFT4I4tXZ9sG6ZWTaj8ohkw1V8M130_assertion evidence source_evidence_literature NP374933.RAbn0b-Le2ZCbecl0oPFT4I4tXZ9sG6ZWTaj8ohkw1V8M130_provenance.
- NP374933.RAbn0b-Le2ZCbecl0oPFT4I4tXZ9sG6ZWTaj8ohkw1V8M130_assertion SIO_000772 16675726 NP374933.RAbn0b-Le2ZCbecl0oPFT4I4tXZ9sG6ZWTaj8ohkw1V8M130_provenance.
- NP374933.RAbn0b-Le2ZCbecl0oPFT4I4tXZ9sG6ZWTaj8ohkw1V8M130_assertion wasDerivedFrom befree-20150227 NP374933.RAbn0b-Le2ZCbecl0oPFT4I4tXZ9sG6ZWTaj8ohkw1V8M130_provenance.
- NP374933.RAbn0b-Le2ZCbecl0oPFT4I4tXZ9sG6ZWTaj8ohkw1V8M130_assertion wasGeneratedBy ECO_0000203 NP374933.RAbn0b-Le2ZCbecl0oPFT4I4tXZ9sG6ZWTaj8ohkw1V8M130_provenance.
- befree-20150227 importedOn "2015-02-27" NP374933.RAbn0b-Le2ZCbecl0oPFT4I4tXZ9sG6ZWTaj8ohkw1V8M130_provenance.