Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP333145.RAHUGxxM3-w_mNSVrfDYRVEv3g3qLKIKEYCgnTviYo8vw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP333145.RAHUGxxM3-w_mNSVrfDYRVEv3g3qLKIKEYCgnTviYo8vw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP333145.RAHUGxxM3-w_mNSVrfDYRVEv3g3qLKIKEYCgnTviYo8vw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP333145.RAHUGxxM3-w_mNSVrfDYRVEv3g3qLKIKEYCgnTviYo8vw130_provenance.
- NP333145.RAHUGxxM3-w_mNSVrfDYRVEv3g3qLKIKEYCgnTviYo8vw130_assertion description "[Mutations in endoglin and activin receptor-like kinase 1 (ALK1), an endothelial specific TGF-beta type I receptor, have been linked to hereditary hemorrhagic telangiectasia (HHT), an autosomal dominant vascular dysplasia characterized by telangiectases and arteriovenous malformations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP333145.RAHUGxxM3-w_mNSVrfDYRVEv3g3qLKIKEYCgnTviYo8vw130_provenance.
- NP333145.RAHUGxxM3-w_mNSVrfDYRVEv3g3qLKIKEYCgnTviYo8vw130_assertion evidence source_evidence_literature NP333145.RAHUGxxM3-w_mNSVrfDYRVEv3g3qLKIKEYCgnTviYo8vw130_provenance.
- NP333145.RAHUGxxM3-w_mNSVrfDYRVEv3g3qLKIKEYCgnTviYo8vw130_assertion SIO_000772 18283546 NP333145.RAHUGxxM3-w_mNSVrfDYRVEv3g3qLKIKEYCgnTviYo8vw130_provenance.
- NP333145.RAHUGxxM3-w_mNSVrfDYRVEv3g3qLKIKEYCgnTviYo8vw130_assertion wasDerivedFrom befree-20140225 NP333145.RAHUGxxM3-w_mNSVrfDYRVEv3g3qLKIKEYCgnTviYo8vw130_provenance.
- NP333145.RAHUGxxM3-w_mNSVrfDYRVEv3g3qLKIKEYCgnTviYo8vw130_assertion wasGeneratedBy ECO_0000203 NP333145.RAHUGxxM3-w_mNSVrfDYRVEv3g3qLKIKEYCgnTviYo8vw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP333145.RAHUGxxM3-w_mNSVrfDYRVEv3g3qLKIKEYCgnTviYo8vw130_provenance.