@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP208900.RAolfEypxe2LN4J7xOIEp9n6fMH6Un1kqersZEYy55kdY
> .
@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:NP208900.RAolfEypxe2LN4J7xOIEp9n6fMH6Un1kqersZEYy55kdY130_head
{
this:
np:hasAssertion
dgn-np:NP208900.RAolfEypxe2LN4J7xOIEp9n6fMH6Un1kqersZEYy55kdY130_assertion
;
np:hasProvenance
dgn-np:NP208900.RAolfEypxe2LN4J7xOIEp9n6fMH6Un1kqersZEYy55kdY130_provenance
;
np:hasPublicationInfo
dgn-np:NP208900.RAolfEypxe2LN4J7xOIEp9n6fMH6Un1kqersZEYy55kdY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP208900.RAolfEypxe2LN4J7xOIEp9n6fMH6Un1kqersZEYy55kdY130_assertion
a
np:Assertion
.
dgn-np:NP208900.RAolfEypxe2LN4J7xOIEp9n6fMH6Un1kqersZEYy55kdY130_provenance
a
np:Provenance
.
dgn-np:NP208900.RAolfEypxe2LN4J7xOIEp9n6fMH6Un1kqersZEYy55kdY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP208900.RAolfEypxe2LN4J7xOIEp9n6fMH6Un1kqersZEYy55kdY130_assertion
{
miriam-gene:55655
a
ncit:C16612
.
lld:C0678222
a
ncit:C7057
.
dgn-gda:DGN1a644cefe35e5f7327aa85df577b859b
sio:SIO_000628
miriam-gene:55655
,
lld:C0678222
;
a
sio:SIO_001121
.
}
dgn-np:NP208900.RAolfEypxe2LN4J7xOIEp9n6fMH6Un1kqersZEYy55kdY130_provenance
{
dgn-np:NP208900.RAolfEypxe2LN4J7xOIEp9n6fMH6Un1kqersZEYy55kdY130_assertion
dcterms:description
"[In Poland founder alleles of the BRCA1, CHEK2 and NBS1 genes have been associated with an increased risk of breast cancer, but the relative contribution of each of these alleles to the overall breast cancer burden has not yet been determined.]. 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:15980987
;
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:NP208900.RAolfEypxe2LN4J7xOIEp9n6fMH6Un1kqersZEYy55kdY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:55+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" .
}