@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP193979.RAJM8U4fM9aVpZW2GOpfjZkBd0gTVrUtk6BaRrln0FdhU
> .
@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:NP193979.RAJM8U4fM9aVpZW2GOpfjZkBd0gTVrUtk6BaRrln0FdhU130_head
{
this:
np:hasAssertion
dgn-np:NP193979.RAJM8U4fM9aVpZW2GOpfjZkBd0gTVrUtk6BaRrln0FdhU130_assertion
;
np:hasProvenance
dgn-np:NP193979.RAJM8U4fM9aVpZW2GOpfjZkBd0gTVrUtk6BaRrln0FdhU130_provenance
;
np:hasPublicationInfo
dgn-np:NP193979.RAJM8U4fM9aVpZW2GOpfjZkBd0gTVrUtk6BaRrln0FdhU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP193979.RAJM8U4fM9aVpZW2GOpfjZkBd0gTVrUtk6BaRrln0FdhU130_assertion
a
np:Assertion
.
dgn-np:NP193979.RAJM8U4fM9aVpZW2GOpfjZkBd0gTVrUtk6BaRrln0FdhU130_provenance
a
np:Provenance
.
dgn-np:NP193979.RAJM8U4fM9aVpZW2GOpfjZkBd0gTVrUtk6BaRrln0FdhU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP193979.RAJM8U4fM9aVpZW2GOpfjZkBd0gTVrUtk6BaRrln0FdhU130_assertion
{
miriam-gene:3596
a
ncit:C16612
.
lld:C0678222
a
ncit:C7057
.
dgn-gda:DGN07f5572c2d963efeee4458ca44e4247c
sio:SIO_000628
miriam-gene:3596
,
lld:C0678222
;
a
sio:SIO_001121
.
}
dgn-np:NP193979.RAJM8U4fM9aVpZW2GOpfjZkBd0gTVrUtk6BaRrln0FdhU130_provenance
{
dgn-np:NP193979.RAJM8U4fM9aVpZW2GOpfjZkBd0gTVrUtk6BaRrln0FdhU130_assertion
dcterms:description
"[Despite observing no association between breast cancer and the single SNPs, results of this investigation suggest that the presence of CCA haplotype of IL13 gene may be associated with susceptibility of Iranian women to 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:18989750
;
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:NP193979.RAJM8U4fM9aVpZW2GOpfjZkBd0gTVrUtk6BaRrln0FdhU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:47+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" .
}