Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP144812.RACGr37eXO4FkBLOQ5kuM8jD2guuVc4cFDL_sXj2tf9N8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP144812.RACGr37eXO4FkBLOQ5kuM8jD2guuVc4cFDL_sXj2tf9N8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP144812.RACGr37eXO4FkBLOQ5kuM8jD2guuVc4cFDL_sXj2tf9N8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP144812.RACGr37eXO4FkBLOQ5kuM8jD2guuVc4cFDL_sXj2tf9N8130_provenance.
- NP144812.RACGr37eXO4FkBLOQ5kuM8jD2guuVc4cFDL_sXj2tf9N8130_assertion description "[The results indicate that ACTC1 mutations or reduced ACTC1 levels may lead to atrial septal defect without signs of cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144812.RACGr37eXO4FkBLOQ5kuM8jD2guuVc4cFDL_sXj2tf9N8130_provenance.
- NP144812.RACGr37eXO4FkBLOQ5kuM8jD2guuVc4cFDL_sXj2tf9N8130_assertion evidence source_evidence_literature NP144812.RACGr37eXO4FkBLOQ5kuM8jD2guuVc4cFDL_sXj2tf9N8130_provenance.
- NP144812.RACGr37eXO4FkBLOQ5kuM8jD2guuVc4cFDL_sXj2tf9N8130_assertion SIO_000772 17947298 NP144812.RACGr37eXO4FkBLOQ5kuM8jD2guuVc4cFDL_sXj2tf9N8130_provenance.
- NP144812.RACGr37eXO4FkBLOQ5kuM8jD2guuVc4cFDL_sXj2tf9N8130_assertion wasDerivedFrom lhgdn-20090331 NP144812.RACGr37eXO4FkBLOQ5kuM8jD2guuVc4cFDL_sXj2tf9N8130_provenance.
- NP144812.RACGr37eXO4FkBLOQ5kuM8jD2guuVc4cFDL_sXj2tf9N8130_assertion wasGeneratedBy ECO_0000203 NP144812.RACGr37eXO4FkBLOQ5kuM8jD2guuVc4cFDL_sXj2tf9N8130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP144812.RACGr37eXO4FkBLOQ5kuM8jD2guuVc4cFDL_sXj2tf9N8130_provenance.