Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP667803.RAddVK7-TM5pUqg1dfqUO5vZR3NdtiWE6UCmB23Ia0Lhg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP667803.RAddVK7-TM5pUqg1dfqUO5vZR3NdtiWE6UCmB23Ia0Lhg130_assertion type Assertion NP667803.RAddVK7-TM5pUqg1dfqUO5vZR3NdtiWE6UCmB23Ia0Lhg130_head.
- NP667803.RAddVK7-TM5pUqg1dfqUO5vZR3NdtiWE6UCmB23Ia0Lhg130_assertion description "[Fragile X syndrome (FXS) mental retardation is caused by loss-of-function mutations in an RNA-binding protein, fragile X mental retardation protein (FMRP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP667803.RAddVK7-TM5pUqg1dfqUO5vZR3NdtiWE6UCmB23Ia0Lhg130_provenance.
- NP667803.RAddVK7-TM5pUqg1dfqUO5vZR3NdtiWE6UCmB23Ia0Lhg130_assertion evidence source_evidence_literature NP667803.RAddVK7-TM5pUqg1dfqUO5vZR3NdtiWE6UCmB23Ia0Lhg130_provenance.
- NP667803.RAddVK7-TM5pUqg1dfqUO5vZR3NdtiWE6UCmB23Ia0Lhg130_assertion SIO_000772 18272470 NP667803.RAddVK7-TM5pUqg1dfqUO5vZR3NdtiWE6UCmB23Ia0Lhg130_provenance.
- NP667803.RAddVK7-TM5pUqg1dfqUO5vZR3NdtiWE6UCmB23Ia0Lhg130_assertion wasDerivedFrom befree-20150227 NP667803.RAddVK7-TM5pUqg1dfqUO5vZR3NdtiWE6UCmB23Ia0Lhg130_provenance.
- NP667803.RAddVK7-TM5pUqg1dfqUO5vZR3NdtiWE6UCmB23Ia0Lhg130_assertion wasGeneratedBy ECO_0000203 NP667803.RAddVK7-TM5pUqg1dfqUO5vZR3NdtiWE6UCmB23Ia0Lhg130_provenance.