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- NP657004.RAUKIrRldqiFpfiCNWSMRezQvWZFRgmn1Esr2ab_jLz70130_assertion type Assertion NP657004.RAUKIrRldqiFpfiCNWSMRezQvWZFRgmn1Esr2ab_jLz70130_head.
- NP657004.RAUKIrRldqiFpfiCNWSMRezQvWZFRgmn1Esr2ab_jLz70130_assertion wasGeneratedBy ECO_0000203 NP657004.RAUKIrRldqiFpfiCNWSMRezQvWZFRgmn1Esr2ab_jLz70130_provenance.
- NP657004.RAUKIrRldqiFpfiCNWSMRezQvWZFRgmn1Esr2ab_jLz70130_assertion wasDerivedFrom befree-20140225 NP657004.RAUKIrRldqiFpfiCNWSMRezQvWZFRgmn1Esr2ab_jLz70130_provenance.
- NP657004.RAUKIrRldqiFpfiCNWSMRezQvWZFRgmn1Esr2ab_jLz70130_assertion SIO_000772 21668430 NP657004.RAUKIrRldqiFpfiCNWSMRezQvWZFRgmn1Esr2ab_jLz70130_provenance.
- NP657004.RAUKIrRldqiFpfiCNWSMRezQvWZFRgmn1Esr2ab_jLz70130_assertion evidence source_evidence_literature NP657004.RAUKIrRldqiFpfiCNWSMRezQvWZFRgmn1Esr2ab_jLz70130_provenance.
- NP657004.RAUKIrRldqiFpfiCNWSMRezQvWZFRgmn1Esr2ab_jLz70130_assertion description "[Analysis of TGM1, ALOX12B, ALOXE3, NIPAL4 and CYP4F22 in autosomal recessive congenital ichthyosis from Galicia (NW Spain): evidence of founder effects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP657004.RAUKIrRldqiFpfiCNWSMRezQvWZFRgmn1Esr2ab_jLz70130_provenance.