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- NP423471.RAXf6DtYiTDlzhW0nNyOt68T1pvEencyMup5WebGNx0XE130_assertion type Assertion NP423471.RAXf6DtYiTDlzhW0nNyOt68T1pvEencyMup5WebGNx0XE130_head.
- NP423471.RAXf6DtYiTDlzhW0nNyOt68T1pvEencyMup5WebGNx0XE130_assertion description "[Here, we report a family with PXE-like cutaneous features in association with multiple coagulation factor deficiency, an autosomal recessive disorder associated with GGCX mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP423471.RAXf6DtYiTDlzhW0nNyOt68T1pvEencyMup5WebGNx0XE130_provenance.
- NP423471.RAXf6DtYiTDlzhW0nNyOt68T1pvEencyMup5WebGNx0XE130_assertion evidence source_evidence_literature NP423471.RAXf6DtYiTDlzhW0nNyOt68T1pvEencyMup5WebGNx0XE130_provenance.
- NP423471.RAXf6DtYiTDlzhW0nNyOt68T1pvEencyMup5WebGNx0XE130_assertion SIO_000772 18800149 NP423471.RAXf6DtYiTDlzhW0nNyOt68T1pvEencyMup5WebGNx0XE130_provenance.
- NP423471.RAXf6DtYiTDlzhW0nNyOt68T1pvEencyMup5WebGNx0XE130_assertion wasDerivedFrom befree-20150227 NP423471.RAXf6DtYiTDlzhW0nNyOt68T1pvEencyMup5WebGNx0XE130_provenance.
- NP423471.RAXf6DtYiTDlzhW0nNyOt68T1pvEencyMup5WebGNx0XE130_assertion wasGeneratedBy ECO_0000203 NP423471.RAXf6DtYiTDlzhW0nNyOt68T1pvEencyMup5WebGNx0XE130_provenance.