Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP733891.RAkGrL_0OOJUDCVAi-efyVWx6g5cafNaeEl18NGEEVh50130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP733891.RAkGrL_0OOJUDCVAi-efyVWx6g5cafNaeEl18NGEEVh50130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP733891.RAkGrL_0OOJUDCVAi-efyVWx6g5cafNaeEl18NGEEVh50130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP733891.RAkGrL_0OOJUDCVAi-efyVWx6g5cafNaeEl18NGEEVh50130_provenance.
- NP733891.RAkGrL_0OOJUDCVAi-efyVWx6g5cafNaeEl18NGEEVh50130_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." NP733891.RAkGrL_0OOJUDCVAi-efyVWx6g5cafNaeEl18NGEEVh50130_provenance.
- NP733891.RAkGrL_0OOJUDCVAi-efyVWx6g5cafNaeEl18NGEEVh50130_assertion evidence source_evidence_literature NP733891.RAkGrL_0OOJUDCVAi-efyVWx6g5cafNaeEl18NGEEVh50130_provenance.
- NP733891.RAkGrL_0OOJUDCVAi-efyVWx6g5cafNaeEl18NGEEVh50130_assertion SIO_000772 18283546 NP733891.RAkGrL_0OOJUDCVAi-efyVWx6g5cafNaeEl18NGEEVh50130_provenance.
- NP733891.RAkGrL_0OOJUDCVAi-efyVWx6g5cafNaeEl18NGEEVh50130_assertion wasDerivedFrom befree-20150227 NP733891.RAkGrL_0OOJUDCVAi-efyVWx6g5cafNaeEl18NGEEVh50130_provenance.
- NP733891.RAkGrL_0OOJUDCVAi-efyVWx6g5cafNaeEl18NGEEVh50130_assertion wasGeneratedBy ECO_0000203 NP733891.RAkGrL_0OOJUDCVAi-efyVWx6g5cafNaeEl18NGEEVh50130_provenance.
- befree-20150227 importedOn "2015-02-27" NP733891.RAkGrL_0OOJUDCVAi-efyVWx6g5cafNaeEl18NGEEVh50130_provenance.