Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP314932.RA2ju4jnmDuavWCoH2OiS_ePz0mkdzTZLNW-MrCsogZ2k130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP314932.RA2ju4jnmDuavWCoH2OiS_ePz0mkdzTZLNW-MrCsogZ2k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP314932.RA2ju4jnmDuavWCoH2OiS_ePz0mkdzTZLNW-MrCsogZ2k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP314932.RA2ju4jnmDuavWCoH2OiS_ePz0mkdzTZLNW-MrCsogZ2k130_provenance.
- NP314932.RA2ju4jnmDuavWCoH2OiS_ePz0mkdzTZLNW-MrCsogZ2k130_assertion description "[Following the recent discovery that the methyl-CpG binding protein 2 (MECP2) gene located on Xq28 is involved in Rett syndrome (RTT), a wild spectrum of phenotypes, including mental handicap, has been shown to be associated with mutations in MECP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP314932.RA2ju4jnmDuavWCoH2OiS_ePz0mkdzTZLNW-MrCsogZ2k130_provenance.
- NP314932.RA2ju4jnmDuavWCoH2OiS_ePz0mkdzTZLNW-MrCsogZ2k130_assertion evidence source_evidence_literature NP314932.RA2ju4jnmDuavWCoH2OiS_ePz0mkdzTZLNW-MrCsogZ2k130_provenance.
- NP314932.RA2ju4jnmDuavWCoH2OiS_ePz0mkdzTZLNW-MrCsogZ2k130_assertion SIO_000772 11309367 NP314932.RA2ju4jnmDuavWCoH2OiS_ePz0mkdzTZLNW-MrCsogZ2k130_provenance.
- NP314932.RA2ju4jnmDuavWCoH2OiS_ePz0mkdzTZLNW-MrCsogZ2k130_assertion wasDerivedFrom befree-2016 NP314932.RA2ju4jnmDuavWCoH2OiS_ePz0mkdzTZLNW-MrCsogZ2k130_provenance.
- NP314932.RA2ju4jnmDuavWCoH2OiS_ePz0mkdzTZLNW-MrCsogZ2k130_assertion wasGeneratedBy ECO_0000203 NP314932.RA2ju4jnmDuavWCoH2OiS_ePz0mkdzTZLNW-MrCsogZ2k130_provenance.
- befree-2016 importedOn "2016-02-19" NP314932.RA2ju4jnmDuavWCoH2OiS_ePz0mkdzTZLNW-MrCsogZ2k130_provenance.