Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP22397.RAPr8SlwzkS1eDyQniYU2w6DVpaygSgmUFILgYLmx0sQw130_assertion> ?p ?o ?g. }
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- NP22397.RAPr8SlwzkS1eDyQniYU2w6DVpaygSgmUFILgYLmx0sQw130_assertion type Assertion NP22397.RAPr8SlwzkS1eDyQniYU2w6DVpaygSgmUFILgYLmx0sQw130_head.
- NP22397.RAPr8SlwzkS1eDyQniYU2w6DVpaygSgmUFILgYLmx0sQw130_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." NP22397.RAPr8SlwzkS1eDyQniYU2w6DVpaygSgmUFILgYLmx0sQw130_provenance.
- NP22397.RAPr8SlwzkS1eDyQniYU2w6DVpaygSgmUFILgYLmx0sQw130_assertion evidence source_evidence_curated NP22397.RAPr8SlwzkS1eDyQniYU2w6DVpaygSgmUFILgYLmx0sQw130_provenance.
- NP22397.RAPr8SlwzkS1eDyQniYU2w6DVpaygSgmUFILgYLmx0sQw130_assertion SIO_000772 19847644 NP22397.RAPr8SlwzkS1eDyQniYU2w6DVpaygSgmUFILgYLmx0sQw130_provenance.
- NP22397.RAPr8SlwzkS1eDyQniYU2w6DVpaygSgmUFILgYLmx0sQw130_assertion wasDerivedFrom ctd_human-20130708 NP22397.RAPr8SlwzkS1eDyQniYU2w6DVpaygSgmUFILgYLmx0sQw130_provenance.
- NP22397.RAPr8SlwzkS1eDyQniYU2w6DVpaygSgmUFILgYLmx0sQw130_assertion wasGeneratedBy ECO_0000218 NP22397.RAPr8SlwzkS1eDyQniYU2w6DVpaygSgmUFILgYLmx0sQw130_provenance.