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- NP548890.RA3Vh7J7-PK-Puitf1Bpm2AeR_5KPAcAMFk65mHF-4rPw130_assertion type Assertion NP548890.RA3Vh7J7-PK-Puitf1Bpm2AeR_5KPAcAMFk65mHF-4rPw130_head.
- NP548890.RA3Vh7J7-PK-Puitf1Bpm2AeR_5KPAcAMFk65mHF-4rPw130_assertion description "[Fragile X syndrome (FXS) is caused by a full mutation expansion (>200 CGG repeats) in the FMR1 gene that results in a deficiency of the fragile X mental retardation protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP548890.RA3Vh7J7-PK-Puitf1Bpm2AeR_5KPAcAMFk65mHF-4rPw130_provenance.
- NP548890.RA3Vh7J7-PK-Puitf1Bpm2AeR_5KPAcAMFk65mHF-4rPw130_assertion evidence source_evidence_literature NP548890.RA3Vh7J7-PK-Puitf1Bpm2AeR_5KPAcAMFk65mHF-4rPw130_provenance.
- NP548890.RA3Vh7J7-PK-Puitf1Bpm2AeR_5KPAcAMFk65mHF-4rPw130_assertion SIO_000772 16685180 NP548890.RA3Vh7J7-PK-Puitf1Bpm2AeR_5KPAcAMFk65mHF-4rPw130_provenance.
- NP548890.RA3Vh7J7-PK-Puitf1Bpm2AeR_5KPAcAMFk65mHF-4rPw130_assertion wasDerivedFrom befree-2016 NP548890.RA3Vh7J7-PK-Puitf1Bpm2AeR_5KPAcAMFk65mHF-4rPw130_provenance.
- NP548890.RA3Vh7J7-PK-Puitf1Bpm2AeR_5KPAcAMFk65mHF-4rPw130_assertion wasGeneratedBy ECO_0000203 NP548890.RA3Vh7J7-PK-Puitf1Bpm2AeR_5KPAcAMFk65mHF-4rPw130_provenance.