Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP215819.RAiuEsgEoe2u-vQk_kQ-xv6iH_RBcF0AVMFGZmyKmfSDs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP215819.RAiuEsgEoe2u-vQk_kQ-xv6iH_RBcF0AVMFGZmyKmfSDs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP215819.RAiuEsgEoe2u-vQk_kQ-xv6iH_RBcF0AVMFGZmyKmfSDs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP215819.RAiuEsgEoe2u-vQk_kQ-xv6iH_RBcF0AVMFGZmyKmfSDs130_provenance.
- NP215819.RAiuEsgEoe2u-vQk_kQ-xv6iH_RBcF0AVMFGZmyKmfSDs130_assertion description "[Mutations in ACVRL1 gene is associated with symptomatic lung involvement and cerebral abscesses in hereditary hemorrhagic telangiectasia]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP215819.RAiuEsgEoe2u-vQk_kQ-xv6iH_RBcF0AVMFGZmyKmfSDs130_provenance.
- NP215819.RAiuEsgEoe2u-vQk_kQ-xv6iH_RBcF0AVMFGZmyKmfSDs130_assertion evidence source_evidence_literature NP215819.RAiuEsgEoe2u-vQk_kQ-xv6iH_RBcF0AVMFGZmyKmfSDs130_provenance.
- NP215819.RAiuEsgEoe2u-vQk_kQ-xv6iH_RBcF0AVMFGZmyKmfSDs130_assertion SIO_000772 17224686 NP215819.RAiuEsgEoe2u-vQk_kQ-xv6iH_RBcF0AVMFGZmyKmfSDs130_provenance.
- NP215819.RAiuEsgEoe2u-vQk_kQ-xv6iH_RBcF0AVMFGZmyKmfSDs130_assertion wasDerivedFrom lhgdn-20090331 NP215819.RAiuEsgEoe2u-vQk_kQ-xv6iH_RBcF0AVMFGZmyKmfSDs130_provenance.
- NP215819.RAiuEsgEoe2u-vQk_kQ-xv6iH_RBcF0AVMFGZmyKmfSDs130_assertion wasGeneratedBy ECO_0000203 NP215819.RAiuEsgEoe2u-vQk_kQ-xv6iH_RBcF0AVMFGZmyKmfSDs130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP215819.RAiuEsgEoe2u-vQk_kQ-xv6iH_RBcF0AVMFGZmyKmfSDs130_provenance.