Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP777667.RAbNpd4SdG2if7NyPI7Ufjh34ciGkpJC9K_zUyeiVUMAE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP777667.RAbNpd4SdG2if7NyPI7Ufjh34ciGkpJC9K_zUyeiVUMAE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP777667.RAbNpd4SdG2if7NyPI7Ufjh34ciGkpJC9K_zUyeiVUMAE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP777667.RAbNpd4SdG2if7NyPI7Ufjh34ciGkpJC9K_zUyeiVUMAE130_provenance.
- NP777667.RAbNpd4SdG2if7NyPI7Ufjh34ciGkpJC9K_zUyeiVUMAE130_assertion description "[A mutation in the rett syndrome gene, MECP2, causes X-linked mental retardation and progressive spasticity in males.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP777667.RAbNpd4SdG2if7NyPI7Ufjh34ciGkpJC9K_zUyeiVUMAE130_provenance.
- NP777667.RAbNpd4SdG2if7NyPI7Ufjh34ciGkpJC9K_zUyeiVUMAE130_assertion evidence source_evidence_literature NP777667.RAbNpd4SdG2if7NyPI7Ufjh34ciGkpJC9K_zUyeiVUMAE130_provenance.
- NP777667.RAbNpd4SdG2if7NyPI7Ufjh34ciGkpJC9K_zUyeiVUMAE130_assertion SIO_000772 10986043 NP777667.RAbNpd4SdG2if7NyPI7Ufjh34ciGkpJC9K_zUyeiVUMAE130_provenance.
- NP777667.RAbNpd4SdG2if7NyPI7Ufjh34ciGkpJC9K_zUyeiVUMAE130_assertion wasDerivedFrom befree-20140225 NP777667.RAbNpd4SdG2if7NyPI7Ufjh34ciGkpJC9K_zUyeiVUMAE130_provenance.
- NP777667.RAbNpd4SdG2if7NyPI7Ufjh34ciGkpJC9K_zUyeiVUMAE130_assertion wasGeneratedBy ECO_0000203 NP777667.RAbNpd4SdG2if7NyPI7Ufjh34ciGkpJC9K_zUyeiVUMAE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP777667.RAbNpd4SdG2if7NyPI7Ufjh34ciGkpJC9K_zUyeiVUMAE130_provenance.