Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP826223.RATHMaIrDxAXRF38xCtbEdM9akHrNQ33TdX3R4wClxPNI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP826223.RATHMaIrDxAXRF38xCtbEdM9akHrNQ33TdX3R4wClxPNI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP826223.RATHMaIrDxAXRF38xCtbEdM9akHrNQ33TdX3R4wClxPNI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP826223.RATHMaIrDxAXRF38xCtbEdM9akHrNQ33TdX3R4wClxPNI130_provenance.
- NP826223.RATHMaIrDxAXRF38xCtbEdM9akHrNQ33TdX3R4wClxPNI130_assertion description "[Mutations in GATA4 have been related to human congenital heart diseases (CHDs) in several studies, whereas mutations in GATA6 have only recently been reported in patients with persistent truncus arteriosus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP826223.RATHMaIrDxAXRF38xCtbEdM9akHrNQ33TdX3R4wClxPNI130_provenance.
- NP826223.RATHMaIrDxAXRF38xCtbEdM9akHrNQ33TdX3R4wClxPNI130_assertion evidence source_evidence_literature NP826223.RATHMaIrDxAXRF38xCtbEdM9akHrNQ33TdX3R4wClxPNI130_provenance.
- NP826223.RATHMaIrDxAXRF38xCtbEdM9akHrNQ33TdX3R4wClxPNI130_assertion SIO_000772 20631719 NP826223.RATHMaIrDxAXRF38xCtbEdM9akHrNQ33TdX3R4wClxPNI130_provenance.
- NP826223.RATHMaIrDxAXRF38xCtbEdM9akHrNQ33TdX3R4wClxPNI130_assertion wasDerivedFrom befree-2016 NP826223.RATHMaIrDxAXRF38xCtbEdM9akHrNQ33TdX3R4wClxPNI130_provenance.
- NP826223.RATHMaIrDxAXRF38xCtbEdM9akHrNQ33TdX3R4wClxPNI130_assertion wasGeneratedBy ECO_0000203 NP826223.RATHMaIrDxAXRF38xCtbEdM9akHrNQ33TdX3R4wClxPNI130_provenance.
- befree-2016 importedOn "2016-02-19" NP826223.RATHMaIrDxAXRF38xCtbEdM9akHrNQ33TdX3R4wClxPNI130_provenance.