Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP396025.RACIOpFbZoqOYr_rO49Egjm03exom4K5b0ZkfQKXI-2YA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP396025.RACIOpFbZoqOYr_rO49Egjm03exom4K5b0ZkfQKXI-2YA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP396025.RACIOpFbZoqOYr_rO49Egjm03exom4K5b0ZkfQKXI-2YA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP396025.RACIOpFbZoqOYr_rO49Egjm03exom4K5b0ZkfQKXI-2YA130_provenance.
- NP396025.RACIOpFbZoqOYr_rO49Egjm03exom4K5b0ZkfQKXI-2YA130_assertion description "[In this study, patients suspected of having a clinical diagnosis of Marfan Syndrome (MFS), Loeys-Dietz Syndrome (LDS) and Thoracic Aortic Aneurysms and Dissections (TAAD) were referred for genetic testing and examined for mutations in the FBN1, TGF?R1, TGF?R2 and ACTA2 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP396025.RACIOpFbZoqOYr_rO49Egjm03exom4K5b0ZkfQKXI-2YA130_provenance.
- NP396025.RACIOpFbZoqOYr_rO49Egjm03exom4K5b0ZkfQKXI-2YA130_assertion evidence source_evidence_literature NP396025.RACIOpFbZoqOYr_rO49Egjm03exom4K5b0ZkfQKXI-2YA130_provenance.
- NP396025.RACIOpFbZoqOYr_rO49Egjm03exom4K5b0ZkfQKXI-2YA130_assertion SIO_000772 24793577 NP396025.RACIOpFbZoqOYr_rO49Egjm03exom4K5b0ZkfQKXI-2YA130_provenance.
- NP396025.RACIOpFbZoqOYr_rO49Egjm03exom4K5b0ZkfQKXI-2YA130_assertion wasDerivedFrom befree-20150227 NP396025.RACIOpFbZoqOYr_rO49Egjm03exom4K5b0ZkfQKXI-2YA130_provenance.
- NP396025.RACIOpFbZoqOYr_rO49Egjm03exom4K5b0ZkfQKXI-2YA130_assertion wasGeneratedBy ECO_0000203 NP396025.RACIOpFbZoqOYr_rO49Egjm03exom4K5b0ZkfQKXI-2YA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP396025.RACIOpFbZoqOYr_rO49Egjm03exom4K5b0ZkfQKXI-2YA130_provenance.