Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP914004.RAnX-pG0FqpxPrrE-rag_L6a3LYWr-os0Bj3KckFuB2Ug130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP914004.RAnX-pG0FqpxPrrE-rag_L6a3LYWr-os0Bj3KckFuB2Ug130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP914004.RAnX-pG0FqpxPrrE-rag_L6a3LYWr-os0Bj3KckFuB2Ug130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP914004.RAnX-pG0FqpxPrrE-rag_L6a3LYWr-os0Bj3KckFuB2Ug130_provenance.
- NP914004.RAnX-pG0FqpxPrrE-rag_L6a3LYWr-os0Bj3KckFuB2Ug130_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." NP914004.RAnX-pG0FqpxPrrE-rag_L6a3LYWr-os0Bj3KckFuB2Ug130_provenance.
- NP914004.RAnX-pG0FqpxPrrE-rag_L6a3LYWr-os0Bj3KckFuB2Ug130_assertion evidence source_evidence_literature NP914004.RAnX-pG0FqpxPrrE-rag_L6a3LYWr-os0Bj3KckFuB2Ug130_provenance.
- NP914004.RAnX-pG0FqpxPrrE-rag_L6a3LYWr-os0Bj3KckFuB2Ug130_assertion SIO_000772 16675726 NP914004.RAnX-pG0FqpxPrrE-rag_L6a3LYWr-os0Bj3KckFuB2Ug130_provenance.
- NP914004.RAnX-pG0FqpxPrrE-rag_L6a3LYWr-os0Bj3KckFuB2Ug130_assertion wasDerivedFrom befree-20140225 NP914004.RAnX-pG0FqpxPrrE-rag_L6a3LYWr-os0Bj3KckFuB2Ug130_provenance.
- NP914004.RAnX-pG0FqpxPrrE-rag_L6a3LYWr-os0Bj3KckFuB2Ug130_assertion wasGeneratedBy ECO_0000203 NP914004.RAnX-pG0FqpxPrrE-rag_L6a3LYWr-os0Bj3KckFuB2Ug130_provenance.
- befree-20140225 importedOn "2014-02-25" NP914004.RAnX-pG0FqpxPrrE-rag_L6a3LYWr-os0Bj3KckFuB2Ug130_provenance.