Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP208588.RAg0vmZRBGIbZ62f1HRYrR2knyaEAlrBz5zj85EX4dYOw130_assertion> ?p ?o ?g. }
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- NP208588.RAg0vmZRBGIbZ62f1HRYrR2knyaEAlrBz5zj85EX4dYOw130_assertion type Assertion NP208588.RAg0vmZRBGIbZ62f1HRYrR2knyaEAlrBz5zj85EX4dYOw130_head.
- NP208588.RAg0vmZRBGIbZ62f1HRYrR2knyaEAlrBz5zj85EX4dYOw130_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." NP208588.RAg0vmZRBGIbZ62f1HRYrR2knyaEAlrBz5zj85EX4dYOw130_provenance.
- NP208588.RAg0vmZRBGIbZ62f1HRYrR2knyaEAlrBz5zj85EX4dYOw130_assertion evidence source_evidence_literature NP208588.RAg0vmZRBGIbZ62f1HRYrR2knyaEAlrBz5zj85EX4dYOw130_provenance.
- NP208588.RAg0vmZRBGIbZ62f1HRYrR2knyaEAlrBz5zj85EX4dYOw130_assertion SIO_000772 15635078 NP208588.RAg0vmZRBGIbZ62f1HRYrR2knyaEAlrBz5zj85EX4dYOw130_provenance.
- NP208588.RAg0vmZRBGIbZ62f1HRYrR2knyaEAlrBz5zj85EX4dYOw130_assertion wasDerivedFrom lhgdn-20090331 NP208588.RAg0vmZRBGIbZ62f1HRYrR2knyaEAlrBz5zj85EX4dYOw130_provenance.
- NP208588.RAg0vmZRBGIbZ62f1HRYrR2knyaEAlrBz5zj85EX4dYOw130_assertion wasGeneratedBy ECO_0000203 NP208588.RAg0vmZRBGIbZ62f1HRYrR2knyaEAlrBz5zj85EX4dYOw130_provenance.