Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP156121.RA7k9gq8hfCdvAWTlq2sPOfTN2oF5cM9xkJ7boDzjCNck130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP156121.RA7k9gq8hfCdvAWTlq2sPOfTN2oF5cM9xkJ7boDzjCNck130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP156121.RA7k9gq8hfCdvAWTlq2sPOfTN2oF5cM9xkJ7boDzjCNck130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP156121.RA7k9gq8hfCdvAWTlq2sPOfTN2oF5cM9xkJ7boDzjCNck130_provenance.
- NP156121.RA7k9gq8hfCdvAWTlq2sPOfTN2oF5cM9xkJ7boDzjCNck130_assertion description "[The purpose of the study was to report the ocular manifestations and immunohistopathologic description of two rare forms of genodermatosis: congenital dyskeratosis (CD) and erythrokeratodermia variabilis (EKV).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP156121.RA7k9gq8hfCdvAWTlq2sPOfTN2oF5cM9xkJ7boDzjCNck130_provenance.
- NP156121.RA7k9gq8hfCdvAWTlq2sPOfTN2oF5cM9xkJ7boDzjCNck130_assertion evidence source_evidence_literature NP156121.RA7k9gq8hfCdvAWTlq2sPOfTN2oF5cM9xkJ7boDzjCNck130_provenance.
- NP156121.RA7k9gq8hfCdvAWTlq2sPOfTN2oF5cM9xkJ7boDzjCNck130_assertion SIO_000772 9663235 NP156121.RA7k9gq8hfCdvAWTlq2sPOfTN2oF5cM9xkJ7boDzjCNck130_provenance.
- NP156121.RA7k9gq8hfCdvAWTlq2sPOfTN2oF5cM9xkJ7boDzjCNck130_assertion wasDerivedFrom befree-20140225 NP156121.RA7k9gq8hfCdvAWTlq2sPOfTN2oF5cM9xkJ7boDzjCNck130_provenance.
- NP156121.RA7k9gq8hfCdvAWTlq2sPOfTN2oF5cM9xkJ7boDzjCNck130_assertion wasGeneratedBy ECO_0000203 NP156121.RA7k9gq8hfCdvAWTlq2sPOfTN2oF5cM9xkJ7boDzjCNck130_provenance.
- befree-20140225 importedOn "2014-02-25" NP156121.RA7k9gq8hfCdvAWTlq2sPOfTN2oF5cM9xkJ7boDzjCNck130_provenance.