Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP15069.RAdhEVH6MndkbalIauEeaeNU90Y1PkTfH_7M0k4JW6V-Y130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP15069.RAdhEVH6MndkbalIauEeaeNU90Y1PkTfH_7M0k4JW6V-Y130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP15069.RAdhEVH6MndkbalIauEeaeNU90Y1PkTfH_7M0k4JW6V-Y130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP15069.RAdhEVH6MndkbalIauEeaeNU90Y1PkTfH_7M0k4JW6V-Y130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP15069.RAdhEVH6MndkbalIauEeaeNU90Y1PkTfH_7M0k4JW6V-Y130_provenance.
- NP15069.RAdhEVH6MndkbalIauEeaeNU90Y1PkTfH_7M0k4JW6V-Y130_assertion wasGeneratedBy ECO_0000218 NP15069.RAdhEVH6MndkbalIauEeaeNU90Y1PkTfH_7M0k4JW6V-Y130_provenance.
- NP15069.RAdhEVH6MndkbalIauEeaeNU90Y1PkTfH_7M0k4JW6V-Y130_assertion wasDerivedFrom ctd_human-20150221 NP15069.RAdhEVH6MndkbalIauEeaeNU90Y1PkTfH_7M0k4JW6V-Y130_provenance.
- NP15069.RAdhEVH6MndkbalIauEeaeNU90Y1PkTfH_7M0k4JW6V-Y130_assertion SIO_000772 25093829 NP15069.RAdhEVH6MndkbalIauEeaeNU90Y1PkTfH_7M0k4JW6V-Y130_provenance.
- NP15069.RAdhEVH6MndkbalIauEeaeNU90Y1PkTfH_7M0k4JW6V-Y130_assertion evidence source_evidence_curated NP15069.RAdhEVH6MndkbalIauEeaeNU90Y1PkTfH_7M0k4JW6V-Y130_provenance.
- NP15069.RAdhEVH6MndkbalIauEeaeNU90Y1PkTfH_7M0k4JW6V-Y130_assertion description "[We sequenced the coding, 5'UTR, and 3'UTR regions of twelve transcription factor genes implicated in cardiac outflow tract development (NKX2.5, GATA4, ISL1, TBX20, MEF2C, BOP/SMYD1, HAND2, FOXC1, FOXC2, FOXH, FOXA2 and TBX1) in 93 non-syndromic, non-Mendelian TOF cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP15069.RAdhEVH6MndkbalIauEeaeNU90Y1PkTfH_7M0k4JW6V-Y130_provenance.