Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP397681.RAXZs3KK8MVXUy4-4vuH2UWxBrRHTCV4sVHnlmn6DcxLI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP397681.RAXZs3KK8MVXUy4-4vuH2UWxBrRHTCV4sVHnlmn6DcxLI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP397681.RAXZs3KK8MVXUy4-4vuH2UWxBrRHTCV4sVHnlmn6DcxLI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP397681.RAXZs3KK8MVXUy4-4vuH2UWxBrRHTCV4sVHnlmn6DcxLI130_provenance.
- befree-2016 importedOn "2016-02-19" NP397681.RAXZs3KK8MVXUy4-4vuH2UWxBrRHTCV4sVHnlmn6DcxLI130_provenance.
- NP397681.RAXZs3KK8MVXUy4-4vuH2UWxBrRHTCV4sVHnlmn6DcxLI130_assertion wasGeneratedBy ECO_0000203 NP397681.RAXZs3KK8MVXUy4-4vuH2UWxBrRHTCV4sVHnlmn6DcxLI130_provenance.
- NP397681.RAXZs3KK8MVXUy4-4vuH2UWxBrRHTCV4sVHnlmn6DcxLI130_assertion wasDerivedFrom befree-2016 NP397681.RAXZs3KK8MVXUy4-4vuH2UWxBrRHTCV4sVHnlmn6DcxLI130_provenance.
- NP397681.RAXZs3KK8MVXUy4-4vuH2UWxBrRHTCV4sVHnlmn6DcxLI130_assertion SIO_000772 12798584 NP397681.RAXZs3KK8MVXUy4-4vuH2UWxBrRHTCV4sVHnlmn6DcxLI130_provenance.
- NP397681.RAXZs3KK8MVXUy4-4vuH2UWxBrRHTCV4sVHnlmn6DcxLI130_assertion evidence source_evidence_literature NP397681.RAXZs3KK8MVXUy4-4vuH2UWxBrRHTCV4sVHnlmn6DcxLI130_provenance.
- NP397681.RAXZs3KK8MVXUy4-4vuH2UWxBrRHTCV4sVHnlmn6DcxLI130_assertion description "[Mutations in NKX2-5 have been found in families showing secundum ASD and atrioventricular (AV) conduction block and in some individuals with tetralogy of Fallot.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP397681.RAXZs3KK8MVXUy4-4vuH2UWxBrRHTCV4sVHnlmn6DcxLI130_provenance.