Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1231903.RAkgpj4SnEztZzpVxNetECpO4HbYp0Q-ySWTYDPE_T5uQ130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1231903.RAkgpj4SnEztZzpVxNetECpO4HbYp0Q-ySWTYDPE_T5uQ130_assertion type Assertion NP1231903.RAkgpj4SnEztZzpVxNetECpO4HbYp0Q-ySWTYDPE_T5uQ130_head.
- NP1231903.RAkgpj4SnEztZzpVxNetECpO4HbYp0Q-ySWTYDPE_T5uQ130_assertion description "[Mutations in COA6 cause cytochrome c oxidase deficiency and neonatal hypertrophic cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1231903.RAkgpj4SnEztZzpVxNetECpO4HbYp0Q-ySWTYDPE_T5uQ130_provenance.
- NP1231903.RAkgpj4SnEztZzpVxNetECpO4HbYp0Q-ySWTYDPE_T5uQ130_assertion evidence source_evidence_literature NP1231903.RAkgpj4SnEztZzpVxNetECpO4HbYp0Q-ySWTYDPE_T5uQ130_provenance.
- NP1231903.RAkgpj4SnEztZzpVxNetECpO4HbYp0Q-ySWTYDPE_T5uQ130_assertion SIO_000772 25339201 NP1231903.RAkgpj4SnEztZzpVxNetECpO4HbYp0Q-ySWTYDPE_T5uQ130_provenance.
- NP1231903.RAkgpj4SnEztZzpVxNetECpO4HbYp0Q-ySWTYDPE_T5uQ130_assertion wasDerivedFrom befree-2016 NP1231903.RAkgpj4SnEztZzpVxNetECpO4HbYp0Q-ySWTYDPE_T5uQ130_provenance.
- NP1231903.RAkgpj4SnEztZzpVxNetECpO4HbYp0Q-ySWTYDPE_T5uQ130_assertion wasGeneratedBy ECO_0000203 NP1231903.RAkgpj4SnEztZzpVxNetECpO4HbYp0Q-ySWTYDPE_T5uQ130_provenance.