@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP46799.RAGXxu4RmJWlutoHQTMICXJeyxgJ9xw4zhLTm7cg8oYd4
> .
@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:NP46799.RAGXxu4RmJWlutoHQTMICXJeyxgJ9xw4zhLTm7cg8oYd4130_head
{
this:
np:hasAssertion
dgn-np:NP46799.RAGXxu4RmJWlutoHQTMICXJeyxgJ9xw4zhLTm7cg8oYd4130_assertion
;
np:hasProvenance
dgn-np:NP46799.RAGXxu4RmJWlutoHQTMICXJeyxgJ9xw4zhLTm7cg8oYd4130_provenance
;
np:hasPublicationInfo
dgn-np:NP46799.RAGXxu4RmJWlutoHQTMICXJeyxgJ9xw4zhLTm7cg8oYd4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP46799.RAGXxu4RmJWlutoHQTMICXJeyxgJ9xw4zhLTm7cg8oYd4130_assertion
a
np:Assertion
.
dgn-np:NP46799.RAGXxu4RmJWlutoHQTMICXJeyxgJ9xw4zhLTm7cg8oYd4130_provenance
a
np:Provenance
.
dgn-np:NP46799.RAGXxu4RmJWlutoHQTMICXJeyxgJ9xw4zhLTm7cg8oYd4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP46799.RAGXxu4RmJWlutoHQTMICXJeyxgJ9xw4zhLTm7cg8oYd4130_assertion
{
miriam-gene:11200
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGN20500663d78a1d6bc14d9d1db9b507e7
sio:SIO_000628
miriam-gene:11200
,
lld:C0006142
;
a
sio:SIO_001122
.
}
dgn-np:NP46799.RAGXxu4RmJWlutoHQTMICXJeyxgJ9xw4zhLTm7cg8oYd4130_provenance
{
dgn-np:NP46799.RAGXxu4RmJWlutoHQTMICXJeyxgJ9xw4zhLTm7cg8oYd4130_assertion
dcterms:description
"[The 1100delC germline mutation of the CHEK2 gene appears to contribute significantly to the overall breast cancer incidence in some West and North European countries, but seems to be much less frequent among breast cancer patients from other regions of Europe.]. 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:16830057
;
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:NP46799.RAGXxu4RmJWlutoHQTMICXJeyxgJ9xw4zhLTm7cg8oYd4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:21+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" .
}