Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP263796.RARGb99aZ913J3sNYZzdRxmcEdbFC9SLYg1_PYe-2cYoY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP263796.RARGb99aZ913J3sNYZzdRxmcEdbFC9SLYg1_PYe-2cYoY130_assertion type Assertion NP263796.RARGb99aZ913J3sNYZzdRxmcEdbFC9SLYg1_PYe-2cYoY130_head.
- NP263796.RARGb99aZ913J3sNYZzdRxmcEdbFC9SLYg1_PYe-2cYoY130_assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP263796.RARGb99aZ913J3sNYZzdRxmcEdbFC9SLYg1_PYe-2cYoY130_provenance.
- NP263796.RARGb99aZ913J3sNYZzdRxmcEdbFC9SLYg1_PYe-2cYoY130_assertion evidence source_evidence_literature NP263796.RARGb99aZ913J3sNYZzdRxmcEdbFC9SLYg1_PYe-2cYoY130_provenance.
- NP263796.RARGb99aZ913J3sNYZzdRxmcEdbFC9SLYg1_PYe-2cYoY130_assertion SIO_000772 10496225 NP263796.RARGb99aZ913J3sNYZzdRxmcEdbFC9SLYg1_PYe-2cYoY130_provenance.
- NP263796.RARGb99aZ913J3sNYZzdRxmcEdbFC9SLYg1_PYe-2cYoY130_assertion wasDerivedFrom befree-2016 NP263796.RARGb99aZ913J3sNYZzdRxmcEdbFC9SLYg1_PYe-2cYoY130_provenance.
- NP263796.RARGb99aZ913J3sNYZzdRxmcEdbFC9SLYg1_PYe-2cYoY130_assertion wasGeneratedBy ECO_0000203 NP263796.RARGb99aZ913J3sNYZzdRxmcEdbFC9SLYg1_PYe-2cYoY130_provenance.