Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1293567.RAPasqhpxPrRs7ALfyU0jbcgAXKkGHPsYTxWhRaH1VegU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1293567.RAPasqhpxPrRs7ALfyU0jbcgAXKkGHPsYTxWhRaH1VegU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1293567.RAPasqhpxPrRs7ALfyU0jbcgAXKkGHPsYTxWhRaH1VegU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1293567.RAPasqhpxPrRs7ALfyU0jbcgAXKkGHPsYTxWhRaH1VegU130_provenance.
- NP1293567.RAPasqhpxPrRs7ALfyU0jbcgAXKkGHPsYTxWhRaH1VegU130_assertion description "[Rett syndrome (RTT) is a neurodevelopmental disorder caused by mutation of the X-linked MECP2 gene and characterized by developmental regression during the first few years of life.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1293567.RAPasqhpxPrRs7ALfyU0jbcgAXKkGHPsYTxWhRaH1VegU130_provenance.
- NP1293567.RAPasqhpxPrRs7ALfyU0jbcgAXKkGHPsYTxWhRaH1VegU130_assertion evidence source_evidence_literature NP1293567.RAPasqhpxPrRs7ALfyU0jbcgAXKkGHPsYTxWhRaH1VegU130_provenance.
- NP1293567.RAPasqhpxPrRs7ALfyU0jbcgAXKkGHPsYTxWhRaH1VegU130_assertion SIO_000772 26332183 NP1293567.RAPasqhpxPrRs7ALfyU0jbcgAXKkGHPsYTxWhRaH1VegU130_provenance.
- NP1293567.RAPasqhpxPrRs7ALfyU0jbcgAXKkGHPsYTxWhRaH1VegU130_assertion wasDerivedFrom befree-2016 NP1293567.RAPasqhpxPrRs7ALfyU0jbcgAXKkGHPsYTxWhRaH1VegU130_provenance.
- NP1293567.RAPasqhpxPrRs7ALfyU0jbcgAXKkGHPsYTxWhRaH1VegU130_assertion wasGeneratedBy ECO_0000203 NP1293567.RAPasqhpxPrRs7ALfyU0jbcgAXKkGHPsYTxWhRaH1VegU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1293567.RAPasqhpxPrRs7ALfyU0jbcgAXKkGHPsYTxWhRaH1VegU130_provenance.