Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP614780.RAaAM6T53Er_CirkhkZG4REE9PGEtvfjbpirQtzLRHPdY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP614780.RAaAM6T53Er_CirkhkZG4REE9PGEtvfjbpirQtzLRHPdY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP614780.RAaAM6T53Er_CirkhkZG4REE9PGEtvfjbpirQtzLRHPdY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP614780.RAaAM6T53Er_CirkhkZG4REE9PGEtvfjbpirQtzLRHPdY130_provenance.
- NP614780.RAaAM6T53Er_CirkhkZG4REE9PGEtvfjbpirQtzLRHPdY130_assertion description "[The conclusion that DLX5 is a direct target of MeCP2 has implications for research on the molecular bases of Rett syndrome, autism, and genomic imprinting.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP614780.RAaAM6T53Er_CirkhkZG4REE9PGEtvfjbpirQtzLRHPdY130_provenance.
- NP614780.RAaAM6T53Er_CirkhkZG4REE9PGEtvfjbpirQtzLRHPdY130_assertion evidence source_evidence_literature NP614780.RAaAM6T53Er_CirkhkZG4REE9PGEtvfjbpirQtzLRHPdY130_provenance.
- NP614780.RAaAM6T53Er_CirkhkZG4REE9PGEtvfjbpirQtzLRHPdY130_assertion SIO_000772 17701895 NP614780.RAaAM6T53Er_CirkhkZG4REE9PGEtvfjbpirQtzLRHPdY130_provenance.
- NP614780.RAaAM6T53Er_CirkhkZG4REE9PGEtvfjbpirQtzLRHPdY130_assertion wasDerivedFrom befree-20140225 NP614780.RAaAM6T53Er_CirkhkZG4REE9PGEtvfjbpirQtzLRHPdY130_provenance.
- NP614780.RAaAM6T53Er_CirkhkZG4REE9PGEtvfjbpirQtzLRHPdY130_assertion wasGeneratedBy ECO_0000203 NP614780.RAaAM6T53Er_CirkhkZG4REE9PGEtvfjbpirQtzLRHPdY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP614780.RAaAM6T53Er_CirkhkZG4REE9PGEtvfjbpirQtzLRHPdY130_provenance.