Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP21859.RAWONE7Bgy7AFsxvGr4g8eU1uygW_vzk9CGkN98t6EWjI130_assertion> ?p ?o ?g. }
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- NP21859.RAWONE7Bgy7AFsxvGr4g8eU1uygW_vzk9CGkN98t6EWjI130_assertion type Assertion NP21859.RAWONE7Bgy7AFsxvGr4g8eU1uygW_vzk9CGkN98t6EWjI130_head.
- 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.