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- source_evidence_literature type ECO_0000212 NP576617.RAL_SiVOPqSQldOE4dF3W7CqFOJp4iNBaJoM75LCpnbLE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP576617.RAL_SiVOPqSQldOE4dF3W7CqFOJp4iNBaJoM75LCpnbLE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP576617.RAL_SiVOPqSQldOE4dF3W7CqFOJp4iNBaJoM75LCpnbLE130_provenance.
- NP576617.RAL_SiVOPqSQldOE4dF3W7CqFOJp4iNBaJoM75LCpnbLE130_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." NP576617.RAL_SiVOPqSQldOE4dF3W7CqFOJp4iNBaJoM75LCpnbLE130_provenance.
- NP576617.RAL_SiVOPqSQldOE4dF3W7CqFOJp4iNBaJoM75LCpnbLE130_assertion evidence source_evidence_literature NP576617.RAL_SiVOPqSQldOE4dF3W7CqFOJp4iNBaJoM75LCpnbLE130_provenance.
- NP576617.RAL_SiVOPqSQldOE4dF3W7CqFOJp4iNBaJoM75LCpnbLE130_assertion SIO_000772 24568867 NP576617.RAL_SiVOPqSQldOE4dF3W7CqFOJp4iNBaJoM75LCpnbLE130_provenance.
- NP576617.RAL_SiVOPqSQldOE4dF3W7CqFOJp4iNBaJoM75LCpnbLE130_assertion wasDerivedFrom befree-20150227 NP576617.RAL_SiVOPqSQldOE4dF3W7CqFOJp4iNBaJoM75LCpnbLE130_provenance.
- NP576617.RAL_SiVOPqSQldOE4dF3W7CqFOJp4iNBaJoM75LCpnbLE130_assertion wasGeneratedBy ECO_0000203 NP576617.RAL_SiVOPqSQldOE4dF3W7CqFOJp4iNBaJoM75LCpnbLE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP576617.RAL_SiVOPqSQldOE4dF3W7CqFOJp4iNBaJoM75LCpnbLE130_provenance.