@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP656488.RA3c9ZabpXhIyqB-s1saumhQrBoqrB20v1eH8St_ZyLYQ> .
@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:NP656488.RA3c9ZabpXhIyqB-s1saumhQrBoqrB20v1eH8St_ZyLYQ130_head {
  this: np:hasAssertion dgn-np:NP656488.RA3c9ZabpXhIyqB-s1saumhQrBoqrB20v1eH8St_ZyLYQ130_assertion ;
    np:hasProvenance dgn-np:NP656488.RA3c9ZabpXhIyqB-s1saumhQrBoqrB20v1eH8St_ZyLYQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP656488.RA3c9ZabpXhIyqB-s1saumhQrBoqrB20v1eH8St_ZyLYQ130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP656488.RA3c9ZabpXhIyqB-s1saumhQrBoqrB20v1eH8St_ZyLYQ130_assertion a np:Assertion .
  dgn-np:NP656488.RA3c9ZabpXhIyqB-s1saumhQrBoqrB20v1eH8St_ZyLYQ130_provenance a np:Provenance .
  dgn-np:NP656488.RA3c9ZabpXhIyqB-s1saumhQrBoqrB20v1eH8St_ZyLYQ130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP656488.RA3c9ZabpXhIyqB-s1saumhQrBoqrB20v1eH8St_ZyLYQ130_assertion {
  miriam-gene:57876 a ncit:C16612 .
  lld:C0010346 a ncit:C7057 .
  dgn-gda:DGN324d52d3a624e3b11ee95bb29b545db4 sio:SIO_000628 miriam-gene:57876 , lld:C0010346 ;
    a sio:SIO_001121 .
}
dgn-np:NP656488.RA3c9ZabpXhIyqB-s1saumhQrBoqrB20v1eH8St_ZyLYQ130_provenance {
  dgn-np:NP656488.RA3c9ZabpXhIyqB-s1saumhQrBoqrB20v1eH8St_ZyLYQ130_assertion dcterms:description "[We have also analyzed the single nucleotide polymorphisms (SNPs) in the exonic sequences of the 3' portions of these two genes to investigate whether sequence variations in these regions can cause person-to-person differences in the susceptibility to IBDs, and report here that non-synonymous SNPs of MUC3A, involving a tyrosine residue with a proposed role in cell signaling, may confer genetic predisposition to CD (P = 0.0132).]. 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:11289722 ;
    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:NP656488.RA3c9ZabpXhIyqB-s1saumhQrBoqrB20v1eH8St_ZyLYQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:35+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" .
}