@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP465253.RAeYhP_eMWaodXOUpPorZxDvD1rCG-mxqrHDVpV3ZmvXU
> .
@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:NP465253.RAeYhP_eMWaodXOUpPorZxDvD1rCG-mxqrHDVpV3ZmvXU130_head
{
this:
np:hasAssertion
dgn-np:NP465253.RAeYhP_eMWaodXOUpPorZxDvD1rCG-mxqrHDVpV3ZmvXU130_assertion
;
np:hasProvenance
dgn-np:NP465253.RAeYhP_eMWaodXOUpPorZxDvD1rCG-mxqrHDVpV3ZmvXU130_provenance
;
np:hasPublicationInfo
dgn-np:NP465253.RAeYhP_eMWaodXOUpPorZxDvD1rCG-mxqrHDVpV3ZmvXU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP465253.RAeYhP_eMWaodXOUpPorZxDvD1rCG-mxqrHDVpV3ZmvXU130_assertion
a
np:Assertion
.
dgn-np:NP465253.RAeYhP_eMWaodXOUpPorZxDvD1rCG-mxqrHDVpV3ZmvXU130_provenance
a
np:Provenance
.
dgn-np:NP465253.RAeYhP_eMWaodXOUpPorZxDvD1rCG-mxqrHDVpV3ZmvXU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP465253.RAeYhP_eMWaodXOUpPorZxDvD1rCG-mxqrHDVpV3ZmvXU130_assertion
{
miriam-gene:5091
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGN11c4daaea4de026c648b341e8255adad
sio:SIO_000628
miriam-gene:5091
,
lld:C0006142
;
a
sio:SIO_001121
.
}
dgn-np:NP465253.RAeYhP_eMWaodXOUpPorZxDvD1rCG-mxqrHDVpV3ZmvXU130_provenance
{
dgn-np:NP465253.RAeYhP_eMWaodXOUpPorZxDvD1rCG-mxqrHDVpV3ZmvXU130_assertion
dcterms:description
"[Among women with serum PCB levels above the median of the distribution in the control group, there was increased risk of breast cancer associated with the presence of at least one valine allele, compared with women who were homozygous for the isoleucine alleles (odds ratio, 2.93; 95% confidence interval, 1.17-7.36).]. 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:9950238
;
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:NP465253.RAeYhP_eMWaodXOUpPorZxDvD1rCG-mxqrHDVpV3ZmvXU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:39+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" .
}