Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP406128.RAh1cZOExeO6r9HKIxjATCCb7WoZK5W4Bc65aDHAT7fPg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP406128.RAh1cZOExeO6r9HKIxjATCCb7WoZK5W4Bc65aDHAT7fPg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP406128.RAh1cZOExeO6r9HKIxjATCCb7WoZK5W4Bc65aDHAT7fPg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP406128.RAh1cZOExeO6r9HKIxjATCCb7WoZK5W4Bc65aDHAT7fPg130_provenance.
- NP406128.RAh1cZOExeO6r9HKIxjATCCb7WoZK5W4Bc65aDHAT7fPg130_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." NP406128.RAh1cZOExeO6r9HKIxjATCCb7WoZK5W4Bc65aDHAT7fPg130_provenance.
- NP406128.RAh1cZOExeO6r9HKIxjATCCb7WoZK5W4Bc65aDHAT7fPg130_assertion evidence source_evidence_literature NP406128.RAh1cZOExeO6r9HKIxjATCCb7WoZK5W4Bc65aDHAT7fPg130_provenance.
- NP406128.RAh1cZOExeO6r9HKIxjATCCb7WoZK5W4Bc65aDHAT7fPg130_assertion SIO_000772 12928484 NP406128.RAh1cZOExeO6r9HKIxjATCCb7WoZK5W4Bc65aDHAT7fPg130_provenance.
- NP406128.RAh1cZOExeO6r9HKIxjATCCb7WoZK5W4Bc65aDHAT7fPg130_assertion wasDerivedFrom befree-2016 NP406128.RAh1cZOExeO6r9HKIxjATCCb7WoZK5W4Bc65aDHAT7fPg130_provenance.
- NP406128.RAh1cZOExeO6r9HKIxjATCCb7WoZK5W4Bc65aDHAT7fPg130_assertion wasGeneratedBy ECO_0000203 NP406128.RAh1cZOExeO6r9HKIxjATCCb7WoZK5W4Bc65aDHAT7fPg130_provenance.
- befree-2016 importedOn "2016-02-19" NP406128.RAh1cZOExeO6r9HKIxjATCCb7WoZK5W4Bc65aDHAT7fPg130_provenance.