Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1249637.RAq9s6GVbATAJ58g6rCM7_D7OjH9bx61iOZaBmYf1l2OU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1249637.RAq9s6GVbATAJ58g6rCM7_D7OjH9bx61iOZaBmYf1l2OU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1249637.RAq9s6GVbATAJ58g6rCM7_D7OjH9bx61iOZaBmYf1l2OU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1249637.RAq9s6GVbATAJ58g6rCM7_D7OjH9bx61iOZaBmYf1l2OU130_provenance.
- NP1249637.RAq9s6GVbATAJ58g6rCM7_D7OjH9bx61iOZaBmYf1l2OU130_assertion description "[RGS6: a novel gene associated with congenital cataract, mental retardation, and microcephaly in a Tunisian family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1249637.RAq9s6GVbATAJ58g6rCM7_D7OjH9bx61iOZaBmYf1l2OU130_provenance.
- NP1249637.RAq9s6GVbATAJ58g6rCM7_D7OjH9bx61iOZaBmYf1l2OU130_assertion evidence source_evidence_literature NP1249637.RAq9s6GVbATAJ58g6rCM7_D7OjH9bx61iOZaBmYf1l2OU130_provenance.
- NP1249637.RAq9s6GVbATAJ58g6rCM7_D7OjH9bx61iOZaBmYf1l2OU130_assertion SIO_000772 25525169 NP1249637.RAq9s6GVbATAJ58g6rCM7_D7OjH9bx61iOZaBmYf1l2OU130_provenance.
- NP1249637.RAq9s6GVbATAJ58g6rCM7_D7OjH9bx61iOZaBmYf1l2OU130_assertion wasDerivedFrom befree-2016 NP1249637.RAq9s6GVbATAJ58g6rCM7_D7OjH9bx61iOZaBmYf1l2OU130_provenance.
- NP1249637.RAq9s6GVbATAJ58g6rCM7_D7OjH9bx61iOZaBmYf1l2OU130_assertion wasGeneratedBy ECO_0000203 NP1249637.RAq9s6GVbATAJ58g6rCM7_D7OjH9bx61iOZaBmYf1l2OU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1249637.RAq9s6GVbATAJ58g6rCM7_D7OjH9bx61iOZaBmYf1l2OU130_provenance.