Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP676666.RAo8bi1VJS_WVGHGsxy9D0hUZ2AfM19PROyRCFOb9jnAM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP676666.RAo8bi1VJS_WVGHGsxy9D0hUZ2AfM19PROyRCFOb9jnAM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP676666.RAo8bi1VJS_WVGHGsxy9D0hUZ2AfM19PROyRCFOb9jnAM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP676666.RAo8bi1VJS_WVGHGsxy9D0hUZ2AfM19PROyRCFOb9jnAM130_provenance.
- NP676666.RAo8bi1VJS_WVGHGsxy9D0hUZ2AfM19PROyRCFOb9jnAM130_assertion description "[Novel mutations of the RS1 gene in a cohort of Chinese families with X-linked retinoschisis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP676666.RAo8bi1VJS_WVGHGsxy9D0hUZ2AfM19PROyRCFOb9jnAM130_provenance.
- NP676666.RAo8bi1VJS_WVGHGsxy9D0hUZ2AfM19PROyRCFOb9jnAM130_assertion evidence source_evidence_literature NP676666.RAo8bi1VJS_WVGHGsxy9D0hUZ2AfM19PROyRCFOb9jnAM130_provenance.
- NP676666.RAo8bi1VJS_WVGHGsxy9D0hUZ2AfM19PROyRCFOb9jnAM130_assertion SIO_000772 24505212 NP676666.RAo8bi1VJS_WVGHGsxy9D0hUZ2AfM19PROyRCFOb9jnAM130_provenance.
- NP676666.RAo8bi1VJS_WVGHGsxy9D0hUZ2AfM19PROyRCFOb9jnAM130_assertion wasDerivedFrom befree-20150227 NP676666.RAo8bi1VJS_WVGHGsxy9D0hUZ2AfM19PROyRCFOb9jnAM130_provenance.
- NP676666.RAo8bi1VJS_WVGHGsxy9D0hUZ2AfM19PROyRCFOb9jnAM130_assertion wasGeneratedBy ECO_0000203 NP676666.RAo8bi1VJS_WVGHGsxy9D0hUZ2AfM19PROyRCFOb9jnAM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP676666.RAo8bi1VJS_WVGHGsxy9D0hUZ2AfM19PROyRCFOb9jnAM130_provenance.