Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP126815.RAc7cKb6u4Ze-dBNCwP3mZjYQFJWP_JKH03PCR_BGsAYo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP126815.RAc7cKb6u4Ze-dBNCwP3mZjYQFJWP_JKH03PCR_BGsAYo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP126815.RAc7cKb6u4Ze-dBNCwP3mZjYQFJWP_JKH03PCR_BGsAYo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP126815.RAc7cKb6u4Ze-dBNCwP3mZjYQFJWP_JKH03PCR_BGsAYo130_provenance.
- NP126815.RAc7cKb6u4Ze-dBNCwP3mZjYQFJWP_JKH03PCR_BGsAYo130_assertion wasGeneratedBy ECO_0000203 NP126815.RAc7cKb6u4Ze-dBNCwP3mZjYQFJWP_JKH03PCR_BGsAYo130_provenance.
- NP126815.RAc7cKb6u4Ze-dBNCwP3mZjYQFJWP_JKH03PCR_BGsAYo130_assertion wasDerivedFrom lhgdn-20090331 NP126815.RAc7cKb6u4Ze-dBNCwP3mZjYQFJWP_JKH03PCR_BGsAYo130_provenance.
- NP126815.RAc7cKb6u4Ze-dBNCwP3mZjYQFJWP_JKH03PCR_BGsAYo130_assertion SIO_000772 18412109 NP126815.RAc7cKb6u4Ze-dBNCwP3mZjYQFJWP_JKH03PCR_BGsAYo130_provenance.
- NP126815.RAc7cKb6u4Ze-dBNCwP3mZjYQFJWP_JKH03PCR_BGsAYo130_assertion evidence source_evidence_literature NP126815.RAc7cKb6u4Ze-dBNCwP3mZjYQFJWP_JKH03PCR_BGsAYo130_provenance.
- NP126815.RAc7cKb6u4Ze-dBNCwP3mZjYQFJWP_JKH03PCR_BGsAYo130_assertion description "[data suggest that the CDKL3 gene is a strong candidate for nonsyndromal autosomal dominant mild mental retardation ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP126815.RAc7cKb6u4Ze-dBNCwP3mZjYQFJWP_JKH03PCR_BGsAYo130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP126815.RAc7cKb6u4Ze-dBNCwP3mZjYQFJWP_JKH03PCR_BGsAYo130_provenance.