Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP597169.RAzHrhVkJ1uGlhgK_5hft3YewhfM9SPgUv1dzDomeZ_g8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP597169.RAzHrhVkJ1uGlhgK_5hft3YewhfM9SPgUv1dzDomeZ_g8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP597169.RAzHrhVkJ1uGlhgK_5hft3YewhfM9SPgUv1dzDomeZ_g8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP597169.RAzHrhVkJ1uGlhgK_5hft3YewhfM9SPgUv1dzDomeZ_g8130_provenance.
- NP597169.RAzHrhVkJ1uGlhgK_5hft3YewhfM9SPgUv1dzDomeZ_g8130_assertion description "[It is necessary to distinguish between lethal mutations leading to diseases such as MCAD and LQTS, and polymorphisms (for instance, in the IL-10 gene and mtDNA) that are normal gene variants but might be suboptimal in critical situations and thus predispose infants to sudden infant death.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP597169.RAzHrhVkJ1uGlhgK_5hft3YewhfM9SPgUv1dzDomeZ_g8130_provenance.
- NP597169.RAzHrhVkJ1uGlhgK_5hft3YewhfM9SPgUv1dzDomeZ_g8130_assertion evidence source_evidence_literature NP597169.RAzHrhVkJ1uGlhgK_5hft3YewhfM9SPgUv1dzDomeZ_g8130_provenance.
- NP597169.RAzHrhVkJ1uGlhgK_5hft3YewhfM9SPgUv1dzDomeZ_g8130_assertion SIO_000772 15466077 NP597169.RAzHrhVkJ1uGlhgK_5hft3YewhfM9SPgUv1dzDomeZ_g8130_provenance.
- NP597169.RAzHrhVkJ1uGlhgK_5hft3YewhfM9SPgUv1dzDomeZ_g8130_assertion wasDerivedFrom befree-20140225 NP597169.RAzHrhVkJ1uGlhgK_5hft3YewhfM9SPgUv1dzDomeZ_g8130_provenance.
- NP597169.RAzHrhVkJ1uGlhgK_5hft3YewhfM9SPgUv1dzDomeZ_g8130_assertion wasGeneratedBy ECO_0000203 NP597169.RAzHrhVkJ1uGlhgK_5hft3YewhfM9SPgUv1dzDomeZ_g8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP597169.RAzHrhVkJ1uGlhgK_5hft3YewhfM9SPgUv1dzDomeZ_g8130_provenance.