Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP294997.RAfO2W9Zucwfe4EQPfzPSSibtZF3F_X11UvTQrgdFtz00130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP294997.RAfO2W9Zucwfe4EQPfzPSSibtZF3F_X11UvTQrgdFtz00130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP294997.RAfO2W9Zucwfe4EQPfzPSSibtZF3F_X11UvTQrgdFtz00130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP294997.RAfO2W9Zucwfe4EQPfzPSSibtZF3F_X11UvTQrgdFtz00130_provenance.
- NP294997.RAfO2W9Zucwfe4EQPfzPSSibtZF3F_X11UvTQrgdFtz00130_assertion description "[The two males and the two obligate carrier females presented a mutation in the MECP2 gene, demonstrating that, in males, MECP2 can be responsible for severe mental retardation associated with neurological disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294997.RAfO2W9Zucwfe4EQPfzPSSibtZF3F_X11UvTQrgdFtz00130_provenance.
- NP294997.RAfO2W9Zucwfe4EQPfzPSSibtZF3F_X11UvTQrgdFtz00130_assertion evidence source_evidence_literature NP294997.RAfO2W9Zucwfe4EQPfzPSSibtZF3F_X11UvTQrgdFtz00130_provenance.
- NP294997.RAfO2W9Zucwfe4EQPfzPSSibtZF3F_X11UvTQrgdFtz00130_assertion SIO_000772 10986043 NP294997.RAfO2W9Zucwfe4EQPfzPSSibtZF3F_X11UvTQrgdFtz00130_provenance.
- NP294997.RAfO2W9Zucwfe4EQPfzPSSibtZF3F_X11UvTQrgdFtz00130_assertion wasDerivedFrom befree-2016 NP294997.RAfO2W9Zucwfe4EQPfzPSSibtZF3F_X11UvTQrgdFtz00130_provenance.
- NP294997.RAfO2W9Zucwfe4EQPfzPSSibtZF3F_X11UvTQrgdFtz00130_assertion wasGeneratedBy ECO_0000203 NP294997.RAfO2W9Zucwfe4EQPfzPSSibtZF3F_X11UvTQrgdFtz00130_provenance.
- befree-2016 importedOn "2016-02-19" NP294997.RAfO2W9Zucwfe4EQPfzPSSibtZF3F_X11UvTQrgdFtz00130_provenance.