Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP423471.RAXf6DtYiTDlzhW0nNyOt68T1pvEencyMup5WebGNx0XE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP423471.RAXf6DtYiTDlzhW0nNyOt68T1pvEencyMup5WebGNx0XE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP423471.RAXf6DtYiTDlzhW0nNyOt68T1pvEencyMup5WebGNx0XE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP423471.RAXf6DtYiTDlzhW0nNyOt68T1pvEencyMup5WebGNx0XE130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP423471.RAXf6DtYiTDlzhW0nNyOt68T1pvEencyMup5WebGNx0XE130_provenance.