Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP602734.RAhBTep4IxrpM0Dp91YI9Ep2vf2BN18pYdoliK49i1rTk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP602734.RAhBTep4IxrpM0Dp91YI9Ep2vf2BN18pYdoliK49i1rTk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP602734.RAhBTep4IxrpM0Dp91YI9Ep2vf2BN18pYdoliK49i1rTk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP602734.RAhBTep4IxrpM0Dp91YI9Ep2vf2BN18pYdoliK49i1rTk130_provenance.
- NP602734.RAhBTep4IxrpM0Dp91YI9Ep2vf2BN18pYdoliK49i1rTk130_assertion description "[Additional loci and genes (OPA2, OPA6 and OPA7) are responsible for X-linked or recessive optic atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP602734.RAhBTep4IxrpM0Dp91YI9Ep2vf2BN18pYdoliK49i1rTk130_provenance.
- NP602734.RAhBTep4IxrpM0Dp91YI9Ep2vf2BN18pYdoliK49i1rTk130_assertion evidence source_evidence_literature NP602734.RAhBTep4IxrpM0Dp91YI9Ep2vf2BN18pYdoliK49i1rTk130_provenance.
- NP602734.RAhBTep4IxrpM0Dp91YI9Ep2vf2BN18pYdoliK49i1rTk130_assertion SIO_000772 22776096 NP602734.RAhBTep4IxrpM0Dp91YI9Ep2vf2BN18pYdoliK49i1rTk130_provenance.
- NP602734.RAhBTep4IxrpM0Dp91YI9Ep2vf2BN18pYdoliK49i1rTk130_assertion wasDerivedFrom befree-20150227 NP602734.RAhBTep4IxrpM0Dp91YI9Ep2vf2BN18pYdoliK49i1rTk130_provenance.
- NP602734.RAhBTep4IxrpM0Dp91YI9Ep2vf2BN18pYdoliK49i1rTk130_assertion wasGeneratedBy ECO_0000203 NP602734.RAhBTep4IxrpM0Dp91YI9Ep2vf2BN18pYdoliK49i1rTk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP602734.RAhBTep4IxrpM0Dp91YI9Ep2vf2BN18pYdoliK49i1rTk130_provenance.