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- NP136056.RA0u2a1LUboHRJJGt37HGtDMNW3wEZ0W5jecVgoki8eng130_assertion type Assertion NP136056.RA0u2a1LUboHRJJGt37HGtDMNW3wEZ0W5jecVgoki8eng130_head.
- NP136056.RA0u2a1LUboHRJJGt37HGtDMNW3wEZ0W5jecVgoki8eng130_assertion wasGeneratedBy ECO_0000203 NP136056.RA0u2a1LUboHRJJGt37HGtDMNW3wEZ0W5jecVgoki8eng130_provenance.
- NP136056.RA0u2a1LUboHRJJGt37HGtDMNW3wEZ0W5jecVgoki8eng130_assertion wasDerivedFrom lhgdn-20090331 NP136056.RA0u2a1LUboHRJJGt37HGtDMNW3wEZ0W5jecVgoki8eng130_provenance.
- NP136056.RA0u2a1LUboHRJJGt37HGtDMNW3wEZ0W5jecVgoki8eng130_assertion SIO_000772 11857753 NP136056.RA0u2a1LUboHRJJGt37HGtDMNW3wEZ0W5jecVgoki8eng130_provenance.
- NP136056.RA0u2a1LUboHRJJGt37HGtDMNW3wEZ0W5jecVgoki8eng130_assertion evidence source_evidence_literature NP136056.RA0u2a1LUboHRJJGt37HGtDMNW3wEZ0W5jecVgoki8eng130_provenance.
- NP136056.RA0u2a1LUboHRJJGt37HGtDMNW3wEZ0W5jecVgoki8eng130_assertion description "[Frataxin and cardiac troponin T gene mutations co-exist in a child with Friedreich ataxia and familial hypertrophic cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136056.RA0u2a1LUboHRJJGt37HGtDMNW3wEZ0W5jecVgoki8eng130_provenance.