Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP320463.RA2EeKCaEv8C4Xed_EduXFqRF1D38KHwiQkCu1UWlROOg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP320463.RA2EeKCaEv8C4Xed_EduXFqRF1D38KHwiQkCu1UWlROOg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP320463.RA2EeKCaEv8C4Xed_EduXFqRF1D38KHwiQkCu1UWlROOg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP320463.RA2EeKCaEv8C4Xed_EduXFqRF1D38KHwiQkCu1UWlROOg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP320463.RA2EeKCaEv8C4Xed_EduXFqRF1D38KHwiQkCu1UWlROOg130_provenance.
- NP320463.RA2EeKCaEv8C4Xed_EduXFqRF1D38KHwiQkCu1UWlROOg130_assertion wasGeneratedBy ECO_0000203 NP320463.RA2EeKCaEv8C4Xed_EduXFqRF1D38KHwiQkCu1UWlROOg130_provenance.
- NP320463.RA2EeKCaEv8C4Xed_EduXFqRF1D38KHwiQkCu1UWlROOg130_assertion wasDerivedFrom befree-20150227 NP320463.RA2EeKCaEv8C4Xed_EduXFqRF1D38KHwiQkCu1UWlROOg130_provenance.
- NP320463.RA2EeKCaEv8C4Xed_EduXFqRF1D38KHwiQkCu1UWlROOg130_assertion SIO_000772 10408773 NP320463.RA2EeKCaEv8C4Xed_EduXFqRF1D38KHwiQkCu1UWlROOg130_provenance.
- NP320463.RA2EeKCaEv8C4Xed_EduXFqRF1D38KHwiQkCu1UWlROOg130_assertion evidence source_evidence_literature NP320463.RA2EeKCaEv8C4Xed_EduXFqRF1D38KHwiQkCu1UWlROOg130_provenance.
- NP320463.RA2EeKCaEv8C4Xed_EduXFqRF1D38KHwiQkCu1UWlROOg130_assertion description "[The Hallopeau-Siemens variant of recessive dystrophic epidermolysis bullosa (HS-RDEB) is a severe inherited skin disease characterized by the absence of collagen type VII (COLVII) and anchoring fibrils (AF), caused by mutations in collagen type VII gene (COL7A1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320463.RA2EeKCaEv8C4Xed_EduXFqRF1D38KHwiQkCu1UWlROOg130_provenance.