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- NP667799.RAieY5RAVO8tMY_h_Ku6JWOijidhWRE1HCh63Ph2dTTqI130_assertion type Assertion NP667799.RAieY5RAVO8tMY_h_Ku6JWOijidhWRE1HCh63Ph2dTTqI130_head.
- NP667799.RAieY5RAVO8tMY_h_Ku6JWOijidhWRE1HCh63Ph2dTTqI130_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." NP667799.RAieY5RAVO8tMY_h_Ku6JWOijidhWRE1HCh63Ph2dTTqI130_provenance.
- NP667799.RAieY5RAVO8tMY_h_Ku6JWOijidhWRE1HCh63Ph2dTTqI130_assertion evidence source_evidence_literature NP667799.RAieY5RAVO8tMY_h_Ku6JWOijidhWRE1HCh63Ph2dTTqI130_provenance.
- NP667799.RAieY5RAVO8tMY_h_Ku6JWOijidhWRE1HCh63Ph2dTTqI130_assertion SIO_000772 10496225 NP667799.RAieY5RAVO8tMY_h_Ku6JWOijidhWRE1HCh63Ph2dTTqI130_provenance.
- NP667799.RAieY5RAVO8tMY_h_Ku6JWOijidhWRE1HCh63Ph2dTTqI130_assertion wasDerivedFrom befree-20150227 NP667799.RAieY5RAVO8tMY_h_Ku6JWOijidhWRE1HCh63Ph2dTTqI130_provenance.
- NP667799.RAieY5RAVO8tMY_h_Ku6JWOijidhWRE1HCh63Ph2dTTqI130_assertion wasGeneratedBy ECO_0000203 NP667799.RAieY5RAVO8tMY_h_Ku6JWOijidhWRE1HCh63Ph2dTTqI130_provenance.