Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP892384.RAExRSx3rFVlYF0e-8UUDMQOxLd6fc5YEhu5EJJvMUU7s130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP892384.RAExRSx3rFVlYF0e-8UUDMQOxLd6fc5YEhu5EJJvMUU7s130_assertion type Assertion NP892384.RAExRSx3rFVlYF0e-8UUDMQOxLd6fc5YEhu5EJJvMUU7s130_head.
- NP892384.RAExRSx3rFVlYF0e-8UUDMQOxLd6fc5YEhu5EJJvMUU7s130_assertion description "[Patients with multiple endocrine neoplasia (MEN) type 2 with known RET gene mutations as well as those with other heritable disorders are candidates for PGD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP892384.RAExRSx3rFVlYF0e-8UUDMQOxLd6fc5YEhu5EJJvMUU7s130_provenance.
- NP892384.RAExRSx3rFVlYF0e-8UUDMQOxLd6fc5YEhu5EJJvMUU7s130_assertion evidence source_evidence_literature NP892384.RAExRSx3rFVlYF0e-8UUDMQOxLd6fc5YEhu5EJJvMUU7s130_provenance.
- NP892384.RAExRSx3rFVlYF0e-8UUDMQOxLd6fc5YEhu5EJJvMUU7s130_assertion SIO_000772 21550946 NP892384.RAExRSx3rFVlYF0e-8UUDMQOxLd6fc5YEhu5EJJvMUU7s130_provenance.
- NP892384.RAExRSx3rFVlYF0e-8UUDMQOxLd6fc5YEhu5EJJvMUU7s130_assertion wasDerivedFrom befree-2016 NP892384.RAExRSx3rFVlYF0e-8UUDMQOxLd6fc5YEhu5EJJvMUU7s130_provenance.
- NP892384.RAExRSx3rFVlYF0e-8UUDMQOxLd6fc5YEhu5EJJvMUU7s130_assertion wasGeneratedBy ECO_0000203 NP892384.RAExRSx3rFVlYF0e-8UUDMQOxLd6fc5YEhu5EJJvMUU7s130_provenance.