Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP620502.RAeQEHCVrR2vo8CAwaQ2obb0kEP9qKl2KBZfYCjzh5CEU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP620502.RAeQEHCVrR2vo8CAwaQ2obb0kEP9qKl2KBZfYCjzh5CEU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP620502.RAeQEHCVrR2vo8CAwaQ2obb0kEP9qKl2KBZfYCjzh5CEU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP620502.RAeQEHCVrR2vo8CAwaQ2obb0kEP9qKl2KBZfYCjzh5CEU130_provenance.
- NP620502.RAeQEHCVrR2vo8CAwaQ2obb0kEP9qKl2KBZfYCjzh5CEU130_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." NP620502.RAeQEHCVrR2vo8CAwaQ2obb0kEP9qKl2KBZfYCjzh5CEU130_provenance.
- NP620502.RAeQEHCVrR2vo8CAwaQ2obb0kEP9qKl2KBZfYCjzh5CEU130_assertion evidence source_evidence_literature NP620502.RAeQEHCVrR2vo8CAwaQ2obb0kEP9qKl2KBZfYCjzh5CEU130_provenance.
- NP620502.RAeQEHCVrR2vo8CAwaQ2obb0kEP9qKl2KBZfYCjzh5CEU130_assertion SIO_000772 16675726 NP620502.RAeQEHCVrR2vo8CAwaQ2obb0kEP9qKl2KBZfYCjzh5CEU130_provenance.
- NP620502.RAeQEHCVrR2vo8CAwaQ2obb0kEP9qKl2KBZfYCjzh5CEU130_assertion wasDerivedFrom befree-20140225 NP620502.RAeQEHCVrR2vo8CAwaQ2obb0kEP9qKl2KBZfYCjzh5CEU130_provenance.
- NP620502.RAeQEHCVrR2vo8CAwaQ2obb0kEP9qKl2KBZfYCjzh5CEU130_assertion wasGeneratedBy ECO_0000203 NP620502.RAeQEHCVrR2vo8CAwaQ2obb0kEP9qKl2KBZfYCjzh5CEU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP620502.RAeQEHCVrR2vo8CAwaQ2obb0kEP9qKl2KBZfYCjzh5CEU130_provenance.