@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP84111.RAle1KsZMqadY-oyEnBFiAi4MaX5Rp_KHgf6I4U0BTntA> .
@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:NP84111.RAle1KsZMqadY-oyEnBFiAi4MaX5Rp_KHgf6I4U0BTntA130_head {
  this: np:hasAssertion dgn-np:NP84111.RAle1KsZMqadY-oyEnBFiAi4MaX5Rp_KHgf6I4U0BTntA130_assertion ;
    np:hasProvenance dgn-np:NP84111.RAle1KsZMqadY-oyEnBFiAi4MaX5Rp_KHgf6I4U0BTntA130_provenance ;
    np:hasPublicationInfo dgn-np:NP84111.RAle1KsZMqadY-oyEnBFiAi4MaX5Rp_KHgf6I4U0BTntA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP84111.RAle1KsZMqadY-oyEnBFiAi4MaX5Rp_KHgf6I4U0BTntA130_assertion a np:Assertion .
  dgn-np:NP84111.RAle1KsZMqadY-oyEnBFiAi4MaX5Rp_KHgf6I4U0BTntA130_provenance a np:Provenance .
  dgn-np:NP84111.RAle1KsZMqadY-oyEnBFiAi4MaX5Rp_KHgf6I4U0BTntA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP84111.RAle1KsZMqadY-oyEnBFiAi4MaX5Rp_KHgf6I4U0BTntA130_assertion {
  miriam-gene:4313 a ncit:C16612 .
  lld:C0027092 a ncit:C7057 .
  dgn-gda:DGNc264927575c66b1f5818176036606d12 sio:SIO_000628 miriam-gene:4313 , lld:C0027092 ;
    a sio:SIO_001122 .
}
dgn-np:NP84111.RAle1KsZMqadY-oyEnBFiAi4MaX5Rp_KHgf6I4U0BTntA130_provenance {
  dgn-np:NP84111.RAle1KsZMqadY-oyEnBFiAi4MaX5Rp_KHgf6I4U0BTntA130_assertion dcterms:description "[Statistically significant genetic associations of ocular refraction to polymorphisms near MMP1 and within MMP2 were identified in the AMISH but not among the ASHK families. The results suggest that the MMP1 and MMP2 genes are involved in refractive variation in the AMISH. Genetic and/or environmental heterogeneity most likely contribute to differences in association results between ethnic groups.]. 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:20484597 ;
    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP84111.RAle1KsZMqadY-oyEnBFiAi4MaX5Rp_KHgf6I4U0BTntA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:41+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" .
}