@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP183508.RAeO7rp3xMzt6H4PyFJQ4sXSroGKeZDO6sUABEMdg5KZc
> .
@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:NP183508.RAeO7rp3xMzt6H4PyFJQ4sXSroGKeZDO6sUABEMdg5KZc130_head
{
this:
np:hasAssertion
dgn-np:NP183508.RAeO7rp3xMzt6H4PyFJQ4sXSroGKeZDO6sUABEMdg5KZc130_assertion
;
np:hasProvenance
dgn-np:NP183508.RAeO7rp3xMzt6H4PyFJQ4sXSroGKeZDO6sUABEMdg5KZc130_provenance
;
np:hasPublicationInfo
dgn-np:NP183508.RAeO7rp3xMzt6H4PyFJQ4sXSroGKeZDO6sUABEMdg5KZc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP183508.RAeO7rp3xMzt6H4PyFJQ4sXSroGKeZDO6sUABEMdg5KZc130_assertion
a
np:Assertion
.
dgn-np:NP183508.RAeO7rp3xMzt6H4PyFJQ4sXSroGKeZDO6sUABEMdg5KZc130_provenance
a
np:Provenance
.
dgn-np:NP183508.RAeO7rp3xMzt6H4PyFJQ4sXSroGKeZDO6sUABEMdg5KZc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP183508.RAeO7rp3xMzt6H4PyFJQ4sXSroGKeZDO6sUABEMdg5KZc130_assertion
{
miriam-gene:2068
a
ncit:C16612
.
lld:C0678222
a
ncit:C7057
.
dgn-gda:DGNca5419ba0de071625533f3587b01ce59
sio:SIO_000628
miriam-gene:2068
,
lld:C0678222
;
a
sio:SIO_001121
.
}
dgn-np:NP183508.RAeO7rp3xMzt6H4PyFJQ4sXSroGKeZDO6sUABEMdg5KZc130_provenance
{
dgn-np:NP183508.RAeO7rp3xMzt6H4PyFJQ4sXSroGKeZDO6sUABEMdg5KZc130_assertion
dcterms:description
"[Five single nucleotide polymorphisms (SNPs) among four XP genes (XPC, XPD, XPF and XPG) were genotyped from DNA samples collected at baseline, and then analyzed by conditional logistic regression for association with the incidence of breast cancer.]. 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:16823510
;
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:NP183508.RAeO7rp3xMzt6H4PyFJQ4sXSroGKeZDO6sUABEMdg5KZc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:39+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" .
}