Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP277426.RAe1ioPI-IdCzyMCPsK0VSSJIM9tYLChWjNye7v_vT0fk130_assertion> ?p ?o ?g. }
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- NP277426.RAe1ioPI-IdCzyMCPsK0VSSJIM9tYLChWjNye7v_vT0fk130_assertion type Assertion NP277426.RAe1ioPI-IdCzyMCPsK0VSSJIM9tYLChWjNye7v_vT0fk130_head.
- 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.