Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1158003.RA6786dSNPfrO30btu6uHqzA3Qv07buGYyAWBxMyIiTaQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1158003.RA6786dSNPfrO30btu6uHqzA3Qv07buGYyAWBxMyIiTaQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1158003.RA6786dSNPfrO30btu6uHqzA3Qv07buGYyAWBxMyIiTaQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1158003.RA6786dSNPfrO30btu6uHqzA3Qv07buGYyAWBxMyIiTaQ130_provenance.
- NP1158003.RA6786dSNPfrO30btu6uHqzA3Qv07buGYyAWBxMyIiTaQ130_assertion description "[ND4L gene concurrent 10609T>C and 10663T>C mutations are associated with Leber's hereditary optic neuropathy in a large pedigree from Kuwait.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1158003.RA6786dSNPfrO30btu6uHqzA3Qv07buGYyAWBxMyIiTaQ130_provenance.
- NP1158003.RA6786dSNPfrO30btu6uHqzA3Qv07buGYyAWBxMyIiTaQ130_assertion evidence source_evidence_literature NP1158003.RA6786dSNPfrO30btu6uHqzA3Qv07buGYyAWBxMyIiTaQ130_provenance.
- NP1158003.RA6786dSNPfrO30btu6uHqzA3Qv07buGYyAWBxMyIiTaQ130_assertion SIO_000772 24568867 NP1158003.RA6786dSNPfrO30btu6uHqzA3Qv07buGYyAWBxMyIiTaQ130_provenance.
- NP1158003.RA6786dSNPfrO30btu6uHqzA3Qv07buGYyAWBxMyIiTaQ130_assertion wasDerivedFrom befree-2016 NP1158003.RA6786dSNPfrO30btu6uHqzA3Qv07buGYyAWBxMyIiTaQ130_provenance.
- NP1158003.RA6786dSNPfrO30btu6uHqzA3Qv07buGYyAWBxMyIiTaQ130_assertion wasGeneratedBy ECO_0000203 NP1158003.RA6786dSNPfrO30btu6uHqzA3Qv07buGYyAWBxMyIiTaQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1158003.RA6786dSNPfrO30btu6uHqzA3Qv07buGYyAWBxMyIiTaQ130_provenance.