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- source_evidence_literature type ECO_0000212 NP295980.RAMKk6acwVtfW0_jx0IKmlhPIj85ezuj8PRLdCDrulhNE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP295980.RAMKk6acwVtfW0_jx0IKmlhPIj85ezuj8PRLdCDrulhNE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP295980.RAMKk6acwVtfW0_jx0IKmlhPIj85ezuj8PRLdCDrulhNE130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP295980.RAMKk6acwVtfW0_jx0IKmlhPIj85ezuj8PRLdCDrulhNE130_provenance.