Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1162557.RA8AT7AikBwOCkW7bTxaGtP116gIGDm72ZwdNxiNbj-tQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1162557.RA8AT7AikBwOCkW7bTxaGtP116gIGDm72ZwdNxiNbj-tQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1162557.RA8AT7AikBwOCkW7bTxaGtP116gIGDm72ZwdNxiNbj-tQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1162557.RA8AT7AikBwOCkW7bTxaGtP116gIGDm72ZwdNxiNbj-tQ130_provenance.
- NP1162557.RA8AT7AikBwOCkW7bTxaGtP116gIGDm72ZwdNxiNbj-tQ130_assertion description "[MECP2 mutations or altered expression are also associated with a spectrum of neurodevelopmental disorders such as autism spectrum disorders with recent links to fetal alcohol spectrum disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1162557.RA8AT7AikBwOCkW7bTxaGtP116gIGDm72ZwdNxiNbj-tQ130_provenance.
- NP1162557.RA8AT7AikBwOCkW7bTxaGtP116gIGDm72ZwdNxiNbj-tQ130_assertion evidence source_evidence_literature NP1162557.RA8AT7AikBwOCkW7bTxaGtP116gIGDm72ZwdNxiNbj-tQ130_provenance.
- NP1162557.RA8AT7AikBwOCkW7bTxaGtP116gIGDm72ZwdNxiNbj-tQ130_assertion SIO_000772 24615633 NP1162557.RA8AT7AikBwOCkW7bTxaGtP116gIGDm72ZwdNxiNbj-tQ130_provenance.
- NP1162557.RA8AT7AikBwOCkW7bTxaGtP116gIGDm72ZwdNxiNbj-tQ130_assertion wasDerivedFrom befree-2016 NP1162557.RA8AT7AikBwOCkW7bTxaGtP116gIGDm72ZwdNxiNbj-tQ130_provenance.
- NP1162557.RA8AT7AikBwOCkW7bTxaGtP116gIGDm72ZwdNxiNbj-tQ130_assertion wasGeneratedBy ECO_0000203 NP1162557.RA8AT7AikBwOCkW7bTxaGtP116gIGDm72ZwdNxiNbj-tQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1162557.RA8AT7AikBwOCkW7bTxaGtP116gIGDm72ZwdNxiNbj-tQ130_provenance.