Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP222461.RAYG_joV4Ef9CXEnTVj5SWs_cQuAA47Wn05s4uXNohFR4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP222461.RAYG_joV4Ef9CXEnTVj5SWs_cQuAA47Wn05s4uXNohFR4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP222461.RAYG_joV4Ef9CXEnTVj5SWs_cQuAA47Wn05s4uXNohFR4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP222461.RAYG_joV4Ef9CXEnTVj5SWs_cQuAA47Wn05s4uXNohFR4130_provenance.
- NP222461.RAYG_joV4Ef9CXEnTVj5SWs_cQuAA47Wn05s4uXNohFR4130_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." NP222461.RAYG_joV4Ef9CXEnTVj5SWs_cQuAA47Wn05s4uXNohFR4130_provenance.
- NP222461.RAYG_joV4Ef9CXEnTVj5SWs_cQuAA47Wn05s4uXNohFR4130_assertion evidence source_evidence_literature NP222461.RAYG_joV4Ef9CXEnTVj5SWs_cQuAA47Wn05s4uXNohFR4130_provenance.
- NP222461.RAYG_joV4Ef9CXEnTVj5SWs_cQuAA47Wn05s4uXNohFR4130_assertion SIO_000772 16675726 NP222461.RAYG_joV4Ef9CXEnTVj5SWs_cQuAA47Wn05s4uXNohFR4130_provenance.
- NP222461.RAYG_joV4Ef9CXEnTVj5SWs_cQuAA47Wn05s4uXNohFR4130_assertion wasDerivedFrom befree-20150227 NP222461.RAYG_joV4Ef9CXEnTVj5SWs_cQuAA47Wn05s4uXNohFR4130_provenance.
- NP222461.RAYG_joV4Ef9CXEnTVj5SWs_cQuAA47Wn05s4uXNohFR4130_assertion wasGeneratedBy ECO_0000203 NP222461.RAYG_joV4Ef9CXEnTVj5SWs_cQuAA47Wn05s4uXNohFR4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP222461.RAYG_joV4Ef9CXEnTVj5SWs_cQuAA47Wn05s4uXNohFR4130_provenance.