Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP126477.RAuCT4szgi141O5_kd7wERyHSpUUpPUl2aVwTgbxfQvzs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP126477.RAuCT4szgi141O5_kd7wERyHSpUUpPUl2aVwTgbxfQvzs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP126477.RAuCT4szgi141O5_kd7wERyHSpUUpPUl2aVwTgbxfQvzs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP126477.RAuCT4szgi141O5_kd7wERyHSpUUpPUl2aVwTgbxfQvzs130_provenance.
- NP126477.RAuCT4szgi141O5_kd7wERyHSpUUpPUl2aVwTgbxfQvzs130_assertion description "[The MEF2A mutations may account for up to 1.93% of the disease population; thus, genetic testing based on mutational analysis of MEF2A may soon be available for many coronary artery disease/myocardial infarction patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP126477.RAuCT4szgi141O5_kd7wERyHSpUUpPUl2aVwTgbxfQvzs130_provenance.
- NP126477.RAuCT4szgi141O5_kd7wERyHSpUUpPUl2aVwTgbxfQvzs130_assertion evidence source_evidence_literature NP126477.RAuCT4szgi141O5_kd7wERyHSpUUpPUl2aVwTgbxfQvzs130_provenance.
- NP126477.RAuCT4szgi141O5_kd7wERyHSpUUpPUl2aVwTgbxfQvzs130_assertion SIO_000772 15861005 NP126477.RAuCT4szgi141O5_kd7wERyHSpUUpPUl2aVwTgbxfQvzs130_provenance.
- NP126477.RAuCT4szgi141O5_kd7wERyHSpUUpPUl2aVwTgbxfQvzs130_assertion wasDerivedFrom lhgdn-20090331 NP126477.RAuCT4szgi141O5_kd7wERyHSpUUpPUl2aVwTgbxfQvzs130_provenance.
- NP126477.RAuCT4szgi141O5_kd7wERyHSpUUpPUl2aVwTgbxfQvzs130_assertion wasGeneratedBy ECO_0000203 NP126477.RAuCT4szgi141O5_kd7wERyHSpUUpPUl2aVwTgbxfQvzs130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP126477.RAuCT4szgi141O5_kd7wERyHSpUUpPUl2aVwTgbxfQvzs130_provenance.