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- source_evidence_literature type ECO_0000212 NP1296693.RAeM40uMxiimemsg_xLuyXwm87Eqs0UF9Aetz-u7J5OGc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1296693.RAeM40uMxiimemsg_xLuyXwm87Eqs0UF9Aetz-u7J5OGc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1296693.RAeM40uMxiimemsg_xLuyXwm87Eqs0UF9Aetz-u7J5OGc130_provenance.
- NP1296693.RAeM40uMxiimemsg_xLuyXwm87Eqs0UF9Aetz-u7J5OGc130_assertion description "[The genes for MAO-A and MAO-B appear to be very close to the Norrie disease gene, on the basis of loss and/or disruption of the MAO genes and activities in atypical Norrie disease patients deleted for the DXS7 locus; linkage among the MAO genes, the Norrie disease gene, and the DXS7 locus; and mapping of all these loci to the chromosomal region Xp11.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1296693.RAeM40uMxiimemsg_xLuyXwm87Eqs0UF9Aetz-u7J5OGc130_provenance.
- NP1296693.RAeM40uMxiimemsg_xLuyXwm87Eqs0UF9Aetz-u7J5OGc130_assertion evidence source_evidence_literature NP1296693.RAeM40uMxiimemsg_xLuyXwm87Eqs0UF9Aetz-u7J5OGc130_provenance.
- NP1296693.RAeM40uMxiimemsg_xLuyXwm87Eqs0UF9Aetz-u7J5OGc130_assertion SIO_000772 2773935 NP1296693.RAeM40uMxiimemsg_xLuyXwm87Eqs0UF9Aetz-u7J5OGc130_provenance.
- NP1296693.RAeM40uMxiimemsg_xLuyXwm87Eqs0UF9Aetz-u7J5OGc130_assertion wasDerivedFrom befree-2016 NP1296693.RAeM40uMxiimemsg_xLuyXwm87Eqs0UF9Aetz-u7J5OGc130_provenance.
- NP1296693.RAeM40uMxiimemsg_xLuyXwm87Eqs0UF9Aetz-u7J5OGc130_assertion wasGeneratedBy ECO_0000203 NP1296693.RAeM40uMxiimemsg_xLuyXwm87Eqs0UF9Aetz-u7J5OGc130_provenance.
- befree-2016 importedOn "2016-02-19" NP1296693.RAeM40uMxiimemsg_xLuyXwm87Eqs0UF9Aetz-u7J5OGc130_provenance.