Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP835483.RAPnIFMxM_E6xFs5luDLdWRtKHzo_o2j3TgE31qgWReGY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP835483.RAPnIFMxM_E6xFs5luDLdWRtKHzo_o2j3TgE31qgWReGY130_assertion type Assertion NP835483.RAPnIFMxM_E6xFs5luDLdWRtKHzo_o2j3TgE31qgWReGY130_head.
- NP835483.RAPnIFMxM_E6xFs5luDLdWRtKHzo_o2j3TgE31qgWReGY130_assertion description "[Our results confirm the significant contribution of ARX mutations in the etiology of MR, especially in this group of patients selected for XLMR (3%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP835483.RAPnIFMxM_E6xFs5luDLdWRtKHzo_o2j3TgE31qgWReGY130_provenance.
- NP835483.RAPnIFMxM_E6xFs5luDLdWRtKHzo_o2j3TgE31qgWReGY130_assertion evidence source_evidence_literature NP835483.RAPnIFMxM_E6xFs5luDLdWRtKHzo_o2j3TgE31qgWReGY130_provenance.
- NP835483.RAPnIFMxM_E6xFs5luDLdWRtKHzo_o2j3TgE31qgWReGY130_assertion SIO_000772 16523516 NP835483.RAPnIFMxM_E6xFs5luDLdWRtKHzo_o2j3TgE31qgWReGY130_provenance.
- NP835483.RAPnIFMxM_E6xFs5luDLdWRtKHzo_o2j3TgE31qgWReGY130_assertion wasDerivedFrom befree-20150227 NP835483.RAPnIFMxM_E6xFs5luDLdWRtKHzo_o2j3TgE31qgWReGY130_provenance.
- NP835483.RAPnIFMxM_E6xFs5luDLdWRtKHzo_o2j3TgE31qgWReGY130_assertion wasGeneratedBy ECO_0000203 NP835483.RAPnIFMxM_E6xFs5luDLdWRtKHzo_o2j3TgE31qgWReGY130_provenance.