Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP760392.RA11O-eBsoTi2C0mpFDuxNLOONzgLScJdp0vGaiH8q7Js130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP760392.RA11O-eBsoTi2C0mpFDuxNLOONzgLScJdp0vGaiH8q7Js130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP760392.RA11O-eBsoTi2C0mpFDuxNLOONzgLScJdp0vGaiH8q7Js130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP760392.RA11O-eBsoTi2C0mpFDuxNLOONzgLScJdp0vGaiH8q7Js130_provenance.
- NP760392.RA11O-eBsoTi2C0mpFDuxNLOONzgLScJdp0vGaiH8q7Js130_assertion description "[Mutations in the gene mitofusin 2 (MFN2) cause the axonal subtype CMT2A, which has also been shown to be associated with optic atrophy, clinical signs of first motor neuron involvement, and early onset stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP760392.RA11O-eBsoTi2C0mpFDuxNLOONzgLScJdp0vGaiH8q7Js130_provenance.
- NP760392.RA11O-eBsoTi2C0mpFDuxNLOONzgLScJdp0vGaiH8q7Js130_assertion evidence source_evidence_literature NP760392.RA11O-eBsoTi2C0mpFDuxNLOONzgLScJdp0vGaiH8q7Js130_provenance.
- NP760392.RA11O-eBsoTi2C0mpFDuxNLOONzgLScJdp0vGaiH8q7Js130_assertion SIO_000772 21258814 NP760392.RA11O-eBsoTi2C0mpFDuxNLOONzgLScJdp0vGaiH8q7Js130_provenance.
- NP760392.RA11O-eBsoTi2C0mpFDuxNLOONzgLScJdp0vGaiH8q7Js130_assertion wasDerivedFrom befree-20140225 NP760392.RA11O-eBsoTi2C0mpFDuxNLOONzgLScJdp0vGaiH8q7Js130_provenance.
- NP760392.RA11O-eBsoTi2C0mpFDuxNLOONzgLScJdp0vGaiH8q7Js130_assertion wasGeneratedBy ECO_0000203 NP760392.RA11O-eBsoTi2C0mpFDuxNLOONzgLScJdp0vGaiH8q7Js130_provenance.
- befree-20140225 importedOn "2014-02-25" NP760392.RA11O-eBsoTi2C0mpFDuxNLOONzgLScJdp0vGaiH8q7Js130_provenance.