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- NP1294643.RAfNd8JGsJnZ5sfNZS_vnYy1GNavDmAWzosqr1tN3F6XQ130_assertion type Assertion NP1294643.RAfNd8JGsJnZ5sfNZS_vnYy1GNavDmAWzosqr1tN3F6XQ130_head.
- NP1294643.RAfNd8JGsJnZ5sfNZS_vnYy1GNavDmAWzosqr1tN3F6XQ130_assertion description "[Genetic variation in MEOX2, but not TCF15, is a strong predictor of CHD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1294643.RAfNd8JGsJnZ5sfNZS_vnYy1GNavDmAWzosqr1tN3F6XQ130_provenance.
- NP1294643.RAfNd8JGsJnZ5sfNZS_vnYy1GNavDmAWzosqr1tN3F6XQ130_assertion evidence source_evidence_literature NP1294643.RAfNd8JGsJnZ5sfNZS_vnYy1GNavDmAWzosqr1tN3F6XQ130_provenance.
- NP1294643.RAfNd8JGsJnZ5sfNZS_vnYy1GNavDmAWzosqr1tN3F6XQ130_assertion SIO_000772 26428460 NP1294643.RAfNd8JGsJnZ5sfNZS_vnYy1GNavDmAWzosqr1tN3F6XQ130_provenance.
- NP1294643.RAfNd8JGsJnZ5sfNZS_vnYy1GNavDmAWzosqr1tN3F6XQ130_assertion wasDerivedFrom befree-2016 NP1294643.RAfNd8JGsJnZ5sfNZS_vnYy1GNavDmAWzosqr1tN3F6XQ130_provenance.
- NP1294643.RAfNd8JGsJnZ5sfNZS_vnYy1GNavDmAWzosqr1tN3F6XQ130_assertion wasGeneratedBy ECO_0000203 NP1294643.RAfNd8JGsJnZ5sfNZS_vnYy1GNavDmAWzosqr1tN3F6XQ130_provenance.