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- NP320342.RAdi59Q2vdrcsNPmVOk6SpThjEDXj06_iBR1_5br-QnSw130_assertion type Assertion NP320342.RAdi59Q2vdrcsNPmVOk6SpThjEDXj06_iBR1_5br-QnSw130_head.
- NP320342.RAdi59Q2vdrcsNPmVOk6SpThjEDXj06_iBR1_5br-QnSw130_assertion wasGeneratedBy ECO_0000203 NP320342.RAdi59Q2vdrcsNPmVOk6SpThjEDXj06_iBR1_5br-QnSw130_provenance.
- NP320342.RAdi59Q2vdrcsNPmVOk6SpThjEDXj06_iBR1_5br-QnSw130_assertion wasDerivedFrom befree-20150227 NP320342.RAdi59Q2vdrcsNPmVOk6SpThjEDXj06_iBR1_5br-QnSw130_provenance.
- NP320342.RAdi59Q2vdrcsNPmVOk6SpThjEDXj06_iBR1_5br-QnSw130_assertion SIO_000772 15563506 NP320342.RAdi59Q2vdrcsNPmVOk6SpThjEDXj06_iBR1_5br-QnSw130_provenance.
- NP320342.RAdi59Q2vdrcsNPmVOk6SpThjEDXj06_iBR1_5br-QnSw130_assertion evidence source_evidence_literature NP320342.RAdi59Q2vdrcsNPmVOk6SpThjEDXj06_iBR1_5br-QnSw130_provenance.
- NP320342.RAdi59Q2vdrcsNPmVOk6SpThjEDXj06_iBR1_5br-QnSw130_assertion description "[This model, where dominant mutations cause mild Bethlem myopathy and recessive mutations cause severe UCMD was recently challenged when a patient with UCMD was shown to have a heterozygous in-frame deletion in COL6A1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320342.RAdi59Q2vdrcsNPmVOk6SpThjEDXj06_iBR1_5br-QnSw130_provenance.