Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP865880.RAyGDhx4zPW80kZ4R25uAe5VhpHlIoMt879GIrs2_VseQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP865880.RAyGDhx4zPW80kZ4R25uAe5VhpHlIoMt879GIrs2_VseQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP865880.RAyGDhx4zPW80kZ4R25uAe5VhpHlIoMt879GIrs2_VseQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP865880.RAyGDhx4zPW80kZ4R25uAe5VhpHlIoMt879GIrs2_VseQ130_provenance.
- NP865880.RAyGDhx4zPW80kZ4R25uAe5VhpHlIoMt879GIrs2_VseQ130_assertion description "[A novel DCC mutation and genetic heterogeneity in congenital mirror movements.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP865880.RAyGDhx4zPW80kZ4R25uAe5VhpHlIoMt879GIrs2_VseQ130_provenance.
- NP865880.RAyGDhx4zPW80kZ4R25uAe5VhpHlIoMt879GIrs2_VseQ130_assertion evidence source_evidence_literature NP865880.RAyGDhx4zPW80kZ4R25uAe5VhpHlIoMt879GIrs2_VseQ130_provenance.
- NP865880.RAyGDhx4zPW80kZ4R25uAe5VhpHlIoMt879GIrs2_VseQ130_assertion SIO_000772 21242494 NP865880.RAyGDhx4zPW80kZ4R25uAe5VhpHlIoMt879GIrs2_VseQ130_provenance.
- NP865880.RAyGDhx4zPW80kZ4R25uAe5VhpHlIoMt879GIrs2_VseQ130_assertion wasDerivedFrom befree-2016 NP865880.RAyGDhx4zPW80kZ4R25uAe5VhpHlIoMt879GIrs2_VseQ130_provenance.
- NP865880.RAyGDhx4zPW80kZ4R25uAe5VhpHlIoMt879GIrs2_VseQ130_assertion wasGeneratedBy ECO_0000203 NP865880.RAyGDhx4zPW80kZ4R25uAe5VhpHlIoMt879GIrs2_VseQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP865880.RAyGDhx4zPW80kZ4R25uAe5VhpHlIoMt879GIrs2_VseQ130_provenance.