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<http://identifiers.org/ncbigene/1913> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C16612> <http://rdf.disgenet.org/nanopublications.trig#NP885325.RAdViS5ucchHv59f3rvAiz6f_nX1HGtIIorWhuYnAEpNY130_assertion> .
<http://linkedlifedata.com/resource/umls/id/C0406704> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C7057> <http://rdf.disgenet.org/nanopublications.trig#NP885325.RAdViS5ucchHv59f3rvAiz6f_nX1HGtIIorWhuYnAEpNY130_assertion> .
<http://rdf.disgenet.org/gene-disease-association.ttl#DGN45a47635769efc2aa8eb9175ea846077> <http://semanticscience.org/resource/SIO_000628> <http://identifiers.org/ncbigene/1913> <http://rdf.disgenet.org/nanopublications.trig#NP885325.RAdViS5ucchHv59f3rvAiz6f_nX1HGtIIorWhuYnAEpNY130_assertion> .
<http://rdf.disgenet.org/gene-disease-association.ttl#DGN45a47635769efc2aa8eb9175ea846077> <http://semanticscience.org/resource/SIO_000628> <http://linkedlifedata.com/resource/umls/id/C0406704> <http://rdf.disgenet.org/nanopublications.trig#NP885325.RAdViS5ucchHv59f3rvAiz6f_nX1HGtIIorWhuYnAEpNY130_assertion> .
<http://rdf.disgenet.org/gene-disease-association.ttl#DGN45a47635769efc2aa8eb9175ea846077> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://semanticscience.org/resource/SIO_001121> <http://rdf.disgenet.org/nanopublications.trig#NP885325.RAdViS5ucchHv59f3rvAiz6f_nX1HGtIIorWhuYnAEpNY130_assertion> .
<http://rdf.disgenet.org/nanopublications.trig#NP885325.RAdViS5ucchHv59f3rvAiz6f_nX1HGtIIorWhuYnAEpNY130_assertion> <http://purl.org/dc/terms/description> "[The EEC syndrome phenotypic severity (EEC score), best-corrected Snellen visual acuity (decimal fraction), slit-lamp biomicroscopy, tear function index, tear breakup time, LSCD, p63 DNA sequence variants, impression cytology, and corneal histopathology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en <http://rdf.disgenet.org/nanopublications.trig#NP885325.RAdViS5ucchHv59f3rvAiz6f_nX1HGtIIorWhuYnAEpNY130_provenance> .
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<http://rdf.disgenet.org/nanopublications.trig#NP885325.RAdViS5ucchHv59f3rvAiz6f_nX1HGtIIorWhuYnAEpNY130_assertion> <http://www.w3.org/ns/prov#wasGeneratedBy> <http://purl.obolibrary.org/obo/eco.owl#ECO_0000203> <http://rdf.disgenet.org/nanopublications.trig#NP885325.RAdViS5ucchHv59f3rvAiz6f_nX1HGtIIorWhuYnAEpNY130_provenance> .
<http://rdf.disgenet.org/v2.1.0/void.ttl#befree-20140225> <http://purl.org/pav/2.0/importedOn> "2014-02-25"^^<http://www.w3.org/2001/XMLSchema#date> <http://rdf.disgenet.org/nanopublications.trig#NP885325.RAdViS5ucchHv59f3rvAiz6f_nX1HGtIIorWhuYnAEpNY130_provenance> .
<http://rdf.disgenet.org/v2.1.0/void.ttl#source_evidence_literature> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://purl.obolibrary.org/obo/eco.owl#ECO_0000212> <http://rdf.disgenet.org/nanopublications.trig#NP885325.RAdViS5ucchHv59f3rvAiz6f_nX1HGtIIorWhuYnAEpNY130_provenance> .
<http://rdf.disgenet.org/v2.1.0/void.ttl#source_evidence_literature> <http://www.w3.org/2000/01/rdf-schema#comment> "Gene-disease associations inferred from text-mining the literature."@en <http://rdf.disgenet.org/nanopublications.trig#NP885325.RAdViS5ucchHv59f3rvAiz6f_nX1HGtIIorWhuYnAEpNY130_provenance> .
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