Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP580183.RANcsS93HFieCaAEdWEzG7YRB_t5uR7bLlH6-1jNBOSyE130_assertion> ?p ?o ?g. }
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- NP580183.RANcsS93HFieCaAEdWEzG7YRB_t5uR7bLlH6-1jNBOSyE130_assertion type Assertion NP580183.RANcsS93HFieCaAEdWEzG7YRB_t5uR7bLlH6-1jNBOSyE130_head.
- NP580183.RANcsS93HFieCaAEdWEzG7YRB_t5uR7bLlH6-1jNBOSyE130_assertion wasGeneratedBy ECO_0000203 NP580183.RANcsS93HFieCaAEdWEzG7YRB_t5uR7bLlH6-1jNBOSyE130_provenance.
- NP580183.RANcsS93HFieCaAEdWEzG7YRB_t5uR7bLlH6-1jNBOSyE130_assertion wasDerivedFrom befree-20140225 NP580183.RANcsS93HFieCaAEdWEzG7YRB_t5uR7bLlH6-1jNBOSyE130_provenance.
- NP580183.RANcsS93HFieCaAEdWEzG7YRB_t5uR7bLlH6-1jNBOSyE130_assertion SIO_000772 15841171 NP580183.RANcsS93HFieCaAEdWEzG7YRB_t5uR7bLlH6-1jNBOSyE130_provenance.
- NP580183.RANcsS93HFieCaAEdWEzG7YRB_t5uR7bLlH6-1jNBOSyE130_assertion evidence source_evidence_literature NP580183.RANcsS93HFieCaAEdWEzG7YRB_t5uR7bLlH6-1jNBOSyE130_provenance.
- NP580183.RANcsS93HFieCaAEdWEzG7YRB_t5uR7bLlH6-1jNBOSyE130_assertion description "[Rare mutations in MEF2A have been proposed as a cause of coronary artery disease (CAD) and myocardial infarction (MI).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP580183.RANcsS93HFieCaAEdWEzG7YRB_t5uR7bLlH6-1jNBOSyE130_provenance.