Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP925446.RAhdUm-eJ0P-h_A0DlVJ0-uZ_tbI70VMs486ahDWj1eB8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP925446.RAhdUm-eJ0P-h_A0DlVJ0-uZ_tbI70VMs486ahDWj1eB8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP925446.RAhdUm-eJ0P-h_A0DlVJ0-uZ_tbI70VMs486ahDWj1eB8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP925446.RAhdUm-eJ0P-h_A0DlVJ0-uZ_tbI70VMs486ahDWj1eB8130_provenance.
- NP925446.RAhdUm-eJ0P-h_A0DlVJ0-uZ_tbI70VMs486ahDWj1eB8130_assertion description "[ACTA2 mutations were identified in 16% of a cohort presenting familial TAAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP925446.RAhdUm-eJ0P-h_A0DlVJ0-uZ_tbI70VMs486ahDWj1eB8130_provenance.
- NP925446.RAhdUm-eJ0P-h_A0DlVJ0-uZ_tbI70VMs486ahDWj1eB8130_assertion evidence source_evidence_literature NP925446.RAhdUm-eJ0P-h_A0DlVJ0-uZ_tbI70VMs486ahDWj1eB8130_provenance.
- NP925446.RAhdUm-eJ0P-h_A0DlVJ0-uZ_tbI70VMs486ahDWj1eB8130_assertion SIO_000772 21937134 NP925446.RAhdUm-eJ0P-h_A0DlVJ0-uZ_tbI70VMs486ahDWj1eB8130_provenance.
- NP925446.RAhdUm-eJ0P-h_A0DlVJ0-uZ_tbI70VMs486ahDWj1eB8130_assertion wasDerivedFrom befree-2016 NP925446.RAhdUm-eJ0P-h_A0DlVJ0-uZ_tbI70VMs486ahDWj1eB8130_provenance.
- NP925446.RAhdUm-eJ0P-h_A0DlVJ0-uZ_tbI70VMs486ahDWj1eB8130_assertion wasGeneratedBy ECO_0000203 NP925446.RAhdUm-eJ0P-h_A0DlVJ0-uZ_tbI70VMs486ahDWj1eB8130_provenance.
- befree-2016 importedOn "2016-02-19" NP925446.RAhdUm-eJ0P-h_A0DlVJ0-uZ_tbI70VMs486ahDWj1eB8130_provenance.