Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP779024.RAn54D4aoYQWh4asfesr0Ros-oiDiluko_VD-udi9PArE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP779024.RAn54D4aoYQWh4asfesr0Ros-oiDiluko_VD-udi9PArE130_assertion type Assertion NP779024.RAn54D4aoYQWh4asfesr0Ros-oiDiluko_VD-udi9PArE130_head.
- NP779024.RAn54D4aoYQWh4asfesr0Ros-oiDiluko_VD-udi9PArE130_assertion description "[Small ring (X) chromosomes lacking the XIST gene at Xq13.2 have been associated with a severe phenotype that includes mental retardation, facial dysmorphism and congenital abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP779024.RAn54D4aoYQWh4asfesr0Ros-oiDiluko_VD-udi9PArE130_provenance.
- NP779024.RAn54D4aoYQWh4asfesr0Ros-oiDiluko_VD-udi9PArE130_assertion evidence source_evidence_literature NP779024.RAn54D4aoYQWh4asfesr0Ros-oiDiluko_VD-udi9PArE130_provenance.
- NP779024.RAn54D4aoYQWh4asfesr0Ros-oiDiluko_VD-udi9PArE130_assertion SIO_000772 10982188 NP779024.RAn54D4aoYQWh4asfesr0Ros-oiDiluko_VD-udi9PArE130_provenance.
- NP779024.RAn54D4aoYQWh4asfesr0Ros-oiDiluko_VD-udi9PArE130_assertion wasDerivedFrom befree-20150227 NP779024.RAn54D4aoYQWh4asfesr0Ros-oiDiluko_VD-udi9PArE130_provenance.
- NP779024.RAn54D4aoYQWh4asfesr0Ros-oiDiluko_VD-udi9PArE130_assertion wasGeneratedBy ECO_0000203 NP779024.RAn54D4aoYQWh4asfesr0Ros-oiDiluko_VD-udi9PArE130_provenance.