Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP295980.RAMKk6acwVtfW0_jx0IKmlhPIj85ezuj8PRLdCDrulhNE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP295980.RAMKk6acwVtfW0_jx0IKmlhPIj85ezuj8PRLdCDrulhNE130_assertion type Assertion NP295980.RAMKk6acwVtfW0_jx0IKmlhPIj85ezuj8PRLdCDrulhNE130_head.
- NP295980.RAMKk6acwVtfW0_jx0IKmlhPIj85ezuj8PRLdCDrulhNE130_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." NP295980.RAMKk6acwVtfW0_jx0IKmlhPIj85ezuj8PRLdCDrulhNE130_provenance.
- NP295980.RAMKk6acwVtfW0_jx0IKmlhPIj85ezuj8PRLdCDrulhNE130_assertion evidence source_evidence_literature NP295980.RAMKk6acwVtfW0_jx0IKmlhPIj85ezuj8PRLdCDrulhNE130_provenance.
- NP295980.RAMKk6acwVtfW0_jx0IKmlhPIj85ezuj8PRLdCDrulhNE130_assertion SIO_000772 10496225 NP295980.RAMKk6acwVtfW0_jx0IKmlhPIj85ezuj8PRLdCDrulhNE130_provenance.
- NP295980.RAMKk6acwVtfW0_jx0IKmlhPIj85ezuj8PRLdCDrulhNE130_assertion wasDerivedFrom befree-20140225 NP295980.RAMKk6acwVtfW0_jx0IKmlhPIj85ezuj8PRLdCDrulhNE130_provenance.
- NP295980.RAMKk6acwVtfW0_jx0IKmlhPIj85ezuj8PRLdCDrulhNE130_assertion wasGeneratedBy ECO_0000203 NP295980.RAMKk6acwVtfW0_jx0IKmlhPIj85ezuj8PRLdCDrulhNE130_provenance.