Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP208587.RAsFCMZN_MiwnlYB42gEmZLuFyH5bXAOh1rVJvjL3U_mY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP208587.RAsFCMZN_MiwnlYB42gEmZLuFyH5bXAOh1rVJvjL3U_mY130_assertion type Assertion NP208587.RAsFCMZN_MiwnlYB42gEmZLuFyH5bXAOh1rVJvjL3U_mY130_head.
- NP208587.RAsFCMZN_MiwnlYB42gEmZLuFyH5bXAOh1rVJvjL3U_mY130_assertion description "[Routine germline MEN1 mutation testing of all cases of " classical " MEN1, familial hyperparathyroidism, and sporadic hyperparathyroidism with one other MEN1 related condition is justified by national testing services.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP208587.RAsFCMZN_MiwnlYB42gEmZLuFyH5bXAOh1rVJvjL3U_mY130_provenance.
- NP208587.RAsFCMZN_MiwnlYB42gEmZLuFyH5bXAOh1rVJvjL3U_mY130_assertion evidence source_evidence_literature NP208587.RAsFCMZN_MiwnlYB42gEmZLuFyH5bXAOh1rVJvjL3U_mY130_provenance.
- NP208587.RAsFCMZN_MiwnlYB42gEmZLuFyH5bXAOh1rVJvjL3U_mY130_assertion SIO_000772 15635078 NP208587.RAsFCMZN_MiwnlYB42gEmZLuFyH5bXAOh1rVJvjL3U_mY130_provenance.
- NP208587.RAsFCMZN_MiwnlYB42gEmZLuFyH5bXAOh1rVJvjL3U_mY130_assertion wasDerivedFrom lhgdn-20090331 NP208587.RAsFCMZN_MiwnlYB42gEmZLuFyH5bXAOh1rVJvjL3U_mY130_provenance.
- NP208587.RAsFCMZN_MiwnlYB42gEmZLuFyH5bXAOh1rVJvjL3U_mY130_assertion wasGeneratedBy ECO_0000203 NP208587.RAsFCMZN_MiwnlYB42gEmZLuFyH5bXAOh1rVJvjL3U_mY130_provenance.