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<http://rdf.disgenet.org/nanopublications.trig#NP652506.RAj_vm7iy9li_yPkh_P6fvFPDr36gpxpgF1iPT0AFEO8I130_publicationInfo> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://www.nanopub.org/nschema#PublicationInfo> <http://rdf.disgenet.org/nanopublications.trig#NP652506.RAj_vm7iy9li_yPkh_P6fvFPDr36gpxpgF1iPT0AFEO8I130_head> .
<http://identifiers.org/ncbigene/4804> <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#NP652506.RAj_vm7iy9li_yPkh_P6fvFPDr36gpxpgF1iPT0AFEO8I130_assertion> .
<http://linkedlifedata.com/resource/umls/id/C0279626> <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#NP652506.RAj_vm7iy9li_yPkh_P6fvFPDr36gpxpgF1iPT0AFEO8I130_assertion> .
<http://rdf.disgenet.org/gene-disease-association.ttl#DGN2e861b076f7f0b476fedcac2f9ff44df> <http://semanticscience.org/resource/SIO_000628> <http://identifiers.org/ncbigene/4804> <http://rdf.disgenet.org/nanopublications.trig#NP652506.RAj_vm7iy9li_yPkh_P6fvFPDr36gpxpgF1iPT0AFEO8I130_assertion> .
<http://rdf.disgenet.org/gene-disease-association.ttl#DGN2e861b076f7f0b476fedcac2f9ff44df> <http://semanticscience.org/resource/SIO_000628> <http://linkedlifedata.com/resource/umls/id/C0279626> <http://rdf.disgenet.org/nanopublications.trig#NP652506.RAj_vm7iy9li_yPkh_P6fvFPDr36gpxpgF1iPT0AFEO8I130_assertion> .
<http://rdf.disgenet.org/gene-disease-association.ttl#DGN2e861b076f7f0b476fedcac2f9ff44df> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://semanticscience.org/resource/SIO_001121> <http://rdf.disgenet.org/nanopublications.trig#NP652506.RAj_vm7iy9li_yPkh_P6fvFPDr36gpxpgF1iPT0AFEO8I130_assertion> .
<http://rdf.disgenet.org/nanopublications.trig#NP652506.RAj_vm7iy9li_yPkh_P6fvFPDr36gpxpgF1iPT0AFEO8I130_assertion> <http://purl.org/dc/terms/description> "[In this study, we investigated the clinicopathologic significance of the low-affinity p75 neurotrophin receptor (p75NTR; which is expressed in the stem/progenitor cell fraction of normal esophageal epithelial cells) in 187 resected esophageal squamous cell carcinoma (ESCC) specimens and found that approximately 50% of ESCC expressed p75NTR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en <http://rdf.disgenet.org/nanopublications.trig#NP652506.RAj_vm7iy9li_yPkh_P6fvFPDr36gpxpgF1iPT0AFEO8I130_provenance> .
<http://rdf.disgenet.org/nanopublications.trig#NP652506.RAj_vm7iy9li_yPkh_P6fvFPDr36gpxpgF1iPT0AFEO8I130_assertion> <http://purl.org/ontology/wi/core#evidence> <http://rdf.disgenet.org/v2.1.0/void.ttl#source_evidence_literature> <http://rdf.disgenet.org/nanopublications.trig#NP652506.RAj_vm7iy9li_yPkh_P6fvFPDr36gpxpgF1iPT0AFEO8I130_provenance> .
<http://rdf.disgenet.org/nanopublications.trig#NP652506.RAj_vm7iy9li_yPkh_P6fvFPDr36gpxpgF1iPT0AFEO8I130_assertion> <http://semanticscience.org/resource/SIO_000772> <http://identifiers.org/pubmed/16951226> <http://rdf.disgenet.org/nanopublications.trig#NP652506.RAj_vm7iy9li_yPkh_P6fvFPDr36gpxpgF1iPT0AFEO8I130_provenance> .
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<http://rdf.disgenet.org/nanopublications.trig#NP652506.RAj_vm7iy9li_yPkh_P6fvFPDr36gpxpgF1iPT0AFEO8I130_assertion> <http://www.w3.org/ns/prov#wasGeneratedBy> <http://purl.obolibrary.org/obo/eco.owl#ECO_0000203> <http://rdf.disgenet.org/nanopublications.trig#NP652506.RAj_vm7iy9li_yPkh_P6fvFPDr36gpxpgF1iPT0AFEO8I130_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#NP652506.RAj_vm7iy9li_yPkh_P6fvFPDr36gpxpgF1iPT0AFEO8I130_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#NP652506.RAj_vm7iy9li_yPkh_P6fvFPDr36gpxpgF1iPT0AFEO8I130_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#NP652506.RAj_vm7iy9li_yPkh_P6fvFPDr36gpxpgF1iPT0AFEO8I130_provenance> .
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