Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP406126.RArrzpHE8sW8GgpEV9ep1GGD0AHfv_sBduSv_s38-iFhE130_assertion> ?p ?o ?g. }
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- NP406126.RArrzpHE8sW8GgpEV9ep1GGD0AHfv_sBduSv_s38-iFhE130_assertion type Assertion NP406126.RArrzpHE8sW8GgpEV9ep1GGD0AHfv_sBduSv_s38-iFhE130_head.
- NP406126.RArrzpHE8sW8GgpEV9ep1GGD0AHfv_sBduSv_s38-iFhE130_assertion description "[Two of the most common clinical presentations, Leigh Syndrome and hypertrophic cardiomyopathy, have so far only been associated with mutations in SURF1 or SCO2 and COX15, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP406126.RArrzpHE8sW8GgpEV9ep1GGD0AHfv_sBduSv_s38-iFhE130_provenance.
- NP406126.RArrzpHE8sW8GgpEV9ep1GGD0AHfv_sBduSv_s38-iFhE130_assertion evidence source_evidence_literature NP406126.RArrzpHE8sW8GgpEV9ep1GGD0AHfv_sBduSv_s38-iFhE130_provenance.
- NP406126.RArrzpHE8sW8GgpEV9ep1GGD0AHfv_sBduSv_s38-iFhE130_assertion SIO_000772 12928484 NP406126.RArrzpHE8sW8GgpEV9ep1GGD0AHfv_sBduSv_s38-iFhE130_provenance.
- NP406126.RArrzpHE8sW8GgpEV9ep1GGD0AHfv_sBduSv_s38-iFhE130_assertion wasDerivedFrom befree-2016 NP406126.RArrzpHE8sW8GgpEV9ep1GGD0AHfv_sBduSv_s38-iFhE130_provenance.
- NP406126.RArrzpHE8sW8GgpEV9ep1GGD0AHfv_sBduSv_s38-iFhE130_assertion wasGeneratedBy ECO_0000203 NP406126.RArrzpHE8sW8GgpEV9ep1GGD0AHfv_sBduSv_s38-iFhE130_provenance.