Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP303301.RARNI6_6p2RLaZNWgSSq1pOaYwm6FdnRaVH6aHFq2KZMc130_assertion> ?p ?o ?g. }
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- NP303301.RARNI6_6p2RLaZNWgSSq1pOaYwm6FdnRaVH6aHFq2KZMc130_assertion type Assertion NP303301.RARNI6_6p2RLaZNWgSSq1pOaYwm6FdnRaVH6aHFq2KZMc130_head.
- NP303301.RARNI6_6p2RLaZNWgSSq1pOaYwm6FdnRaVH6aHFq2KZMc130_assertion description "[Although we have a limited number of patients in our cohort, our data is consistent with others in the literature suggesting that CDKN1B and AIP mutations are extremely rare in MEN1 syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP303301.RARNI6_6p2RLaZNWgSSq1pOaYwm6FdnRaVH6aHFq2KZMc130_provenance.
- NP303301.RARNI6_6p2RLaZNWgSSq1pOaYwm6FdnRaVH6aHFq2KZMc130_assertion evidence source_evidence_literature NP303301.RARNI6_6p2RLaZNWgSSq1pOaYwm6FdnRaVH6aHFq2KZMc130_provenance.
- NP303301.RARNI6_6p2RLaZNWgSSq1pOaYwm6FdnRaVH6aHFq2KZMc130_assertion SIO_000772 18710468 NP303301.RARNI6_6p2RLaZNWgSSq1pOaYwm6FdnRaVH6aHFq2KZMc130_provenance.
- NP303301.RARNI6_6p2RLaZNWgSSq1pOaYwm6FdnRaVH6aHFq2KZMc130_assertion wasDerivedFrom befree-20150227 NP303301.RARNI6_6p2RLaZNWgSSq1pOaYwm6FdnRaVH6aHFq2KZMc130_provenance.
- NP303301.RARNI6_6p2RLaZNWgSSq1pOaYwm6FdnRaVH6aHFq2KZMc130_assertion wasGeneratedBy ECO_0000203 NP303301.RARNI6_6p2RLaZNWgSSq1pOaYwm6FdnRaVH6aHFq2KZMc130_provenance.