Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP277426.RAe1ioPI-IdCzyMCPsK0VSSJIM9tYLChWjNye7v_vT0fk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP277426.RAe1ioPI-IdCzyMCPsK0VSSJIM9tYLChWjNye7v_vT0fk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP277426.RAe1ioPI-IdCzyMCPsK0VSSJIM9tYLChWjNye7v_vT0fk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP277426.RAe1ioPI-IdCzyMCPsK0VSSJIM9tYLChWjNye7v_vT0fk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP277426.RAe1ioPI-IdCzyMCPsK0VSSJIM9tYLChWjNye7v_vT0fk130_provenance.
- NP277426.RAe1ioPI-IdCzyMCPsK0VSSJIM9tYLChWjNye7v_vT0fk130_assertion wasGeneratedBy ECO_0000203 NP277426.RAe1ioPI-IdCzyMCPsK0VSSJIM9tYLChWjNye7v_vT0fk130_provenance.
- NP277426.RAe1ioPI-IdCzyMCPsK0VSSJIM9tYLChWjNye7v_vT0fk130_assertion wasDerivedFrom befree-20150227 NP277426.RAe1ioPI-IdCzyMCPsK0VSSJIM9tYLChWjNye7v_vT0fk130_provenance.
- NP277426.RAe1ioPI-IdCzyMCPsK0VSSJIM9tYLChWjNye7v_vT0fk130_assertion SIO_000772 16505158 NP277426.RAe1ioPI-IdCzyMCPsK0VSSJIM9tYLChWjNye7v_vT0fk130_provenance.
- NP277426.RAe1ioPI-IdCzyMCPsK0VSSJIM9tYLChWjNye7v_vT0fk130_assertion evidence source_evidence_literature NP277426.RAe1ioPI-IdCzyMCPsK0VSSJIM9tYLChWjNye7v_vT0fk130_provenance.
- NP277426.RAe1ioPI-IdCzyMCPsK0VSSJIM9tYLChWjNye7v_vT0fk130_assertion description "[Considering all features, CORDX3 is more similar to other X chromosomal cone-rod dystrophies than to CSNB2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP277426.RAe1ioPI-IdCzyMCPsK0VSSJIM9tYLChWjNye7v_vT0fk130_provenance.