Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP823600.RA_loqF8JU4AQEmkUicBW5teevlPIljzqT-sSga2bspIc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP823600.RA_loqF8JU4AQEmkUicBW5teevlPIljzqT-sSga2bspIc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP823600.RA_loqF8JU4AQEmkUicBW5teevlPIljzqT-sSga2bspIc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP823600.RA_loqF8JU4AQEmkUicBW5teevlPIljzqT-sSga2bspIc130_provenance.
- NP823600.RA_loqF8JU4AQEmkUicBW5teevlPIljzqT-sSga2bspIc130_assertion description "[Further mutation analyses in males with X-linked mental retardation must prove that RSK4 is indeed a novel MRX gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP823600.RA_loqF8JU4AQEmkUicBW5teevlPIljzqT-sSga2bspIc130_provenance.
- NP823600.RA_loqF8JU4AQEmkUicBW5teevlPIljzqT-sSga2bspIc130_assertion evidence source_evidence_literature NP823600.RA_loqF8JU4AQEmkUicBW5teevlPIljzqT-sSga2bspIc130_provenance.
- NP823600.RA_loqF8JU4AQEmkUicBW5teevlPIljzqT-sSga2bspIc130_assertion SIO_000772 10644430 NP823600.RA_loqF8JU4AQEmkUicBW5teevlPIljzqT-sSga2bspIc130_provenance.
- NP823600.RA_loqF8JU4AQEmkUicBW5teevlPIljzqT-sSga2bspIc130_assertion wasDerivedFrom befree-20150227 NP823600.RA_loqF8JU4AQEmkUicBW5teevlPIljzqT-sSga2bspIc130_provenance.
- NP823600.RA_loqF8JU4AQEmkUicBW5teevlPIljzqT-sSga2bspIc130_assertion wasGeneratedBy ECO_0000203 NP823600.RA_loqF8JU4AQEmkUicBW5teevlPIljzqT-sSga2bspIc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP823600.RA_loqF8JU4AQEmkUicBW5teevlPIljzqT-sSga2bspIc130_provenance.