Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP21859.RAWONE7Bgy7AFsxvGr4g8eU1uygW_vzk9CGkN98t6EWjI130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP21859.RAWONE7Bgy7AFsxvGr4g8eU1uygW_vzk9CGkN98t6EWjI130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP21859.RAWONE7Bgy7AFsxvGr4g8eU1uygW_vzk9CGkN98t6EWjI130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP21859.RAWONE7Bgy7AFsxvGr4g8eU1uygW_vzk9CGkN98t6EWjI130_provenance.
- NP21859.RAWONE7Bgy7AFsxvGr4g8eU1uygW_vzk9CGkN98t6EWjI130_assertion description "[Menin is a tumor suppressor encoded by Men1 that is mutated in the human-inherited tumor syndrome multiple endocrine neoplasia type 1 (MEN1); it also serves as a critical link in the recruitment of nuclear receptor-mediated transcription.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP21859.RAWONE7Bgy7AFsxvGr4g8eU1uygW_vzk9CGkN98t6EWjI130_provenance.
- NP21859.RAWONE7Bgy7AFsxvGr4g8eU1uygW_vzk9CGkN98t6EWjI130_assertion evidence source_evidence_curated NP21859.RAWONE7Bgy7AFsxvGr4g8eU1uygW_vzk9CGkN98t6EWjI130_provenance.
- NP21859.RAWONE7Bgy7AFsxvGr4g8eU1uygW_vzk9CGkN98t6EWjI130_assertion SIO_000772 19847644 NP21859.RAWONE7Bgy7AFsxvGr4g8eU1uygW_vzk9CGkN98t6EWjI130_provenance.
- NP21859.RAWONE7Bgy7AFsxvGr4g8eU1uygW_vzk9CGkN98t6EWjI130_assertion wasDerivedFrom ctd_human-20150221 NP21859.RAWONE7Bgy7AFsxvGr4g8eU1uygW_vzk9CGkN98t6EWjI130_provenance.
- NP21859.RAWONE7Bgy7AFsxvGr4g8eU1uygW_vzk9CGkN98t6EWjI130_assertion wasGeneratedBy ECO_0000218 NP21859.RAWONE7Bgy7AFsxvGr4g8eU1uygW_vzk9CGkN98t6EWjI130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP21859.RAWONE7Bgy7AFsxvGr4g8eU1uygW_vzk9CGkN98t6EWjI130_provenance.