Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP941090.RA_vFoQGHNL1sUiA13DQpMp6iIpg42RUixfJbprfDZFcA130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP941090.RA_vFoQGHNL1sUiA13DQpMp6iIpg42RUixfJbprfDZFcA130_assertion type Assertion NP941090.RA_vFoQGHNL1sUiA13DQpMp6iIpg42RUixfJbprfDZFcA130_head.
- NP941090.RA_vFoQGHNL1sUiA13DQpMp6iIpg42RUixfJbprfDZFcA130_assertion description "[A binding partner of Upf3b, RBM8a, is located in the 1q21.1 copy-number variation (CNV) associated with mental retardation, autism [4], schizophrenia [5], and microcephaly [6].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP941090.RA_vFoQGHNL1sUiA13DQpMp6iIpg42RUixfJbprfDZFcA130_provenance.
- NP941090.RA_vFoQGHNL1sUiA13DQpMp6iIpg42RUixfJbprfDZFcA130_assertion evidence source_evidence_literature NP941090.RA_vFoQGHNL1sUiA13DQpMp6iIpg42RUixfJbprfDZFcA130_provenance.
- NP941090.RA_vFoQGHNL1sUiA13DQpMp6iIpg42RUixfJbprfDZFcA130_assertion SIO_000772 23638902 NP941090.RA_vFoQGHNL1sUiA13DQpMp6iIpg42RUixfJbprfDZFcA130_provenance.
- NP941090.RA_vFoQGHNL1sUiA13DQpMp6iIpg42RUixfJbprfDZFcA130_assertion wasDerivedFrom befree-20150227 NP941090.RA_vFoQGHNL1sUiA13DQpMp6iIpg42RUixfJbprfDZFcA130_provenance.
- NP941090.RA_vFoQGHNL1sUiA13DQpMp6iIpg42RUixfJbprfDZFcA130_assertion wasGeneratedBy ECO_0000203 NP941090.RA_vFoQGHNL1sUiA13DQpMp6iIpg42RUixfJbprfDZFcA130_provenance.