Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP352912.RAPJqLnJvPqX1XreKLew_tjQoGLQTft88zmHSrzlx_xHg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP352912.RAPJqLnJvPqX1XreKLew_tjQoGLQTft88zmHSrzlx_xHg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP352912.RAPJqLnJvPqX1XreKLew_tjQoGLQTft88zmHSrzlx_xHg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP352912.RAPJqLnJvPqX1XreKLew_tjQoGLQTft88zmHSrzlx_xHg130_provenance.
- NP352912.RAPJqLnJvPqX1XreKLew_tjQoGLQTft88zmHSrzlx_xHg130_assertion description "[A myocyte enhancer factor 2A (MEF2A) mutation that segregated with coronary artery disease/myocardial infarction (CAD/MI) in a large family has recently been described.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP352912.RAPJqLnJvPqX1XreKLew_tjQoGLQTft88zmHSrzlx_xHg130_provenance.
- NP352912.RAPJqLnJvPqX1XreKLew_tjQoGLQTft88zmHSrzlx_xHg130_assertion evidence source_evidence_literature NP352912.RAPJqLnJvPqX1XreKLew_tjQoGLQTft88zmHSrzlx_xHg130_provenance.
- NP352912.RAPJqLnJvPqX1XreKLew_tjQoGLQTft88zmHSrzlx_xHg130_assertion SIO_000772 15958500 NP352912.RAPJqLnJvPqX1XreKLew_tjQoGLQTft88zmHSrzlx_xHg130_provenance.
- NP352912.RAPJqLnJvPqX1XreKLew_tjQoGLQTft88zmHSrzlx_xHg130_assertion wasDerivedFrom befree-20150227 NP352912.RAPJqLnJvPqX1XreKLew_tjQoGLQTft88zmHSrzlx_xHg130_provenance.
- NP352912.RAPJqLnJvPqX1XreKLew_tjQoGLQTft88zmHSrzlx_xHg130_assertion wasGeneratedBy ECO_0000203 NP352912.RAPJqLnJvPqX1XreKLew_tjQoGLQTft88zmHSrzlx_xHg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP352912.RAPJqLnJvPqX1XreKLew_tjQoGLQTft88zmHSrzlx_xHg130_provenance.