Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP372204.RAMszGnN38ma69sxIHp121cJkSCTbdKK24clL61ZHCIyg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP372204.RAMszGnN38ma69sxIHp121cJkSCTbdKK24clL61ZHCIyg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP372204.RAMszGnN38ma69sxIHp121cJkSCTbdKK24clL61ZHCIyg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP372204.RAMszGnN38ma69sxIHp121cJkSCTbdKK24clL61ZHCIyg130_provenance.
- NP372204.RAMszGnN38ma69sxIHp121cJkSCTbdKK24clL61ZHCIyg130_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." NP372204.RAMszGnN38ma69sxIHp121cJkSCTbdKK24clL61ZHCIyg130_provenance.
- NP372204.RAMszGnN38ma69sxIHp121cJkSCTbdKK24clL61ZHCIyg130_assertion evidence source_evidence_literature NP372204.RAMszGnN38ma69sxIHp121cJkSCTbdKK24clL61ZHCIyg130_provenance.
- NP372204.RAMszGnN38ma69sxIHp121cJkSCTbdKK24clL61ZHCIyg130_assertion SIO_000772 12928484 NP372204.RAMszGnN38ma69sxIHp121cJkSCTbdKK24clL61ZHCIyg130_provenance.
- NP372204.RAMszGnN38ma69sxIHp121cJkSCTbdKK24clL61ZHCIyg130_assertion wasDerivedFrom befree-20140225 NP372204.RAMszGnN38ma69sxIHp121cJkSCTbdKK24clL61ZHCIyg130_provenance.
- NP372204.RAMszGnN38ma69sxIHp121cJkSCTbdKK24clL61ZHCIyg130_assertion wasGeneratedBy ECO_0000203 NP372204.RAMszGnN38ma69sxIHp121cJkSCTbdKK24clL61ZHCIyg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP372204.RAMszGnN38ma69sxIHp121cJkSCTbdKK24clL61ZHCIyg130_provenance.