Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP595488.RAQ6kNZEnYPmtojNjtM_6zHfkRlyz-CIrbLknEAo8_wXM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP595488.RAQ6kNZEnYPmtojNjtM_6zHfkRlyz-CIrbLknEAo8_wXM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP595488.RAQ6kNZEnYPmtojNjtM_6zHfkRlyz-CIrbLknEAo8_wXM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP595488.RAQ6kNZEnYPmtojNjtM_6zHfkRlyz-CIrbLknEAo8_wXM130_provenance.
- NP595488.RAQ6kNZEnYPmtojNjtM_6zHfkRlyz-CIrbLknEAo8_wXM130_assertion description "[Messenger RNA from NIPA1, NIPA2, CYFIP1, and GCP5 was reduced but detectable in the subjects with Prader-Willi syndrome with the TI deletion, supporting biallelic expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP595488.RAQ6kNZEnYPmtojNjtM_6zHfkRlyz-CIrbLknEAo8_wXM130_provenance.
- NP595488.RAQ6kNZEnYPmtojNjtM_6zHfkRlyz-CIrbLknEAo8_wXM130_assertion evidence source_evidence_literature NP595488.RAQ6kNZEnYPmtojNjtM_6zHfkRlyz-CIrbLknEAo8_wXM130_provenance.
- NP595488.RAQ6kNZEnYPmtojNjtM_6zHfkRlyz-CIrbLknEAo8_wXM130_assertion SIO_000772 16982806 NP595488.RAQ6kNZEnYPmtojNjtM_6zHfkRlyz-CIrbLknEAo8_wXM130_provenance.
- NP595488.RAQ6kNZEnYPmtojNjtM_6zHfkRlyz-CIrbLknEAo8_wXM130_assertion wasDerivedFrom befree-20140225 NP595488.RAQ6kNZEnYPmtojNjtM_6zHfkRlyz-CIrbLknEAo8_wXM130_provenance.
- NP595488.RAQ6kNZEnYPmtojNjtM_6zHfkRlyz-CIrbLknEAo8_wXM130_assertion wasGeneratedBy ECO_0000203 NP595488.RAQ6kNZEnYPmtojNjtM_6zHfkRlyz-CIrbLknEAo8_wXM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP595488.RAQ6kNZEnYPmtojNjtM_6zHfkRlyz-CIrbLknEAo8_wXM130_provenance.