@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP167255.RA6pxtFd0L5hW9HPgmVDTEjBqMPhNTZP_KcC8oEG-zvH8> .
@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:NP167255.RA6pxtFd0L5hW9HPgmVDTEjBqMPhNTZP_KcC8oEG-zvH8130_head {
  this: np:hasAssertion dgn-np:NP167255.RA6pxtFd0L5hW9HPgmVDTEjBqMPhNTZP_KcC8oEG-zvH8130_assertion ;
    np:hasProvenance dgn-np:NP167255.RA6pxtFd0L5hW9HPgmVDTEjBqMPhNTZP_KcC8oEG-zvH8130_provenance ;
    np:hasPublicationInfo dgn-np:NP167255.RA6pxtFd0L5hW9HPgmVDTEjBqMPhNTZP_KcC8oEG-zvH8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP167255.RA6pxtFd0L5hW9HPgmVDTEjBqMPhNTZP_KcC8oEG-zvH8130_assertion a np:Assertion .
  dgn-np:NP167255.RA6pxtFd0L5hW9HPgmVDTEjBqMPhNTZP_KcC8oEG-zvH8130_provenance a np:Provenance .
  dgn-np:NP167255.RA6pxtFd0L5hW9HPgmVDTEjBqMPhNTZP_KcC8oEG-zvH8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP167255.RA6pxtFd0L5hW9HPgmVDTEjBqMPhNTZP_KcC8oEG-zvH8130_assertion {
  miriam-gene:8846 a ncit:C16612 .
  lld:C0027126 a ncit:C7057 .
  dgn-gda:DGN92bac552f9087d4f602e15863c4f7a9f sio:SIO_000628 miriam-gene:8846 , lld:C0027126 ;
    a sio:SIO_001121 .
}
dgn-np:NP167255.RA6pxtFd0L5hW9HPgmVDTEjBqMPhNTZP_KcC8oEG-zvH8130_provenance {
  dgn-np:NP167255.RA6pxtFd0L5hW9HPgmVDTEjBqMPhNTZP_KcC8oEG-zvH8130_assertion dcterms:description "[As to linkage relationships of C3 with marker systems and with myotonic dystrophy, there was evidence (most of it first presented at the 6th International Congress of Human Genetics, Jerusalem 1981) for synteny with ABH secretion (Se): C3-Se (males) z = 4.35, theta = 0.12 and with Lewis secretion (LES): C3-LES (males z = 3.63, theta = 0.04).]. 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:6627719 ;
    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:NP167255.RA6pxtFd0L5hW9HPgmVDTEjBqMPhNTZP_KcC8oEG-zvH8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:30+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" .
}