@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP373305.RAxY2N5DYX6yeczWScU11T8l7-xfABtF_xQmpZvcp24qY> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .
dgn-np:NP373305.RAxY2N5DYX6yeczWScU11T8l7-xfABtF_xQmpZvcp24qY130_head {
  this: np:hasAssertion dgn-np:NP373305.RAxY2N5DYX6yeczWScU11T8l7-xfABtF_xQmpZvcp24qY130_assertion ;
    np:hasProvenance dgn-np:NP373305.RAxY2N5DYX6yeczWScU11T8l7-xfABtF_xQmpZvcp24qY130_provenance ;
    np:hasPublicationInfo dgn-np:NP373305.RAxY2N5DYX6yeczWScU11T8l7-xfABtF_xQmpZvcp24qY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP373305.RAxY2N5DYX6yeczWScU11T8l7-xfABtF_xQmpZvcp24qY130_assertion a np:Assertion .
  dgn-np:NP373305.RAxY2N5DYX6yeczWScU11T8l7-xfABtF_xQmpZvcp24qY130_provenance a np:Provenance .
  dgn-np:NP373305.RAxY2N5DYX6yeczWScU11T8l7-xfABtF_xQmpZvcp24qY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP373305.RAxY2N5DYX6yeczWScU11T8l7-xfABtF_xQmpZvcp24qY130_assertion {
  miriam-gene:55660 a ncit:C16612 .
  lld:C0007102 a ncit:C7057 .
  dgn-gda:DGNc8232840499f6000b22b954891103d21 sio:SIO_000628 miriam-gene:55660 , lld:C0007102 ;
    a sio:SIO_001121 .
}
dgn-np:NP373305.RAxY2N5DYX6yeczWScU11T8l7-xfABtF_xQmpZvcp24qY130_provenance {
  dgn-np:NP373305.RAxY2N5DYX6yeczWScU11T8l7-xfABtF_xQmpZvcp24qY130_assertion dcterms:description "[We found that 5' secretor haplotypes known to correlate with moderate and low MBL serum levels exhibited associations with increased risk of colon cancer in African Americans, specifically as driven by two haplotypes, LYPA and LYQC, relative to the referent HYPA haplotype (LYPA: OR, 2.60; 95% CI, 1.33-5.08 and LYQC: OR, 2.28; 95% CI, 1.20-4.30).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
    sio:SIO_000772 miriam-pubmed:22282660 ;
    prov:wasDerivedFrom dgn-void:befree-20140225 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
  dgn-void:source_evidence_literature a eco:ECO_0000212 ;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP373305.RAxY2N5DYX6yeczWScU11T8l7-xfABtF_xQmpZvcp24qY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:38+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269> , <http://orcid.org/0000-0002-7534-7661> , <http://orcid.org/0000-0002-9383-528X> , <http://orcid.org/0000-0003-0169-8159> , <http://orcid.org/0000-0003-1244-7654> ;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}