@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP640747.RAShzmjVZV-sPN4E12DE56HSydGr9GhTfZ-9ezax9MB3c
> .
@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:NP640747.RAShzmjVZV-sPN4E12DE56HSydGr9GhTfZ-9ezax9MB3c130_head
{
this:
np:hasAssertion
dgn-np:NP640747.RAShzmjVZV-sPN4E12DE56HSydGr9GhTfZ-9ezax9MB3c130_assertion
;
np:hasProvenance
dgn-np:NP640747.RAShzmjVZV-sPN4E12DE56HSydGr9GhTfZ-9ezax9MB3c130_provenance
;
np:hasPublicationInfo
dgn-np:NP640747.RAShzmjVZV-sPN4E12DE56HSydGr9GhTfZ-9ezax9MB3c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP640747.RAShzmjVZV-sPN4E12DE56HSydGr9GhTfZ-9ezax9MB3c130_assertion
a
np:Assertion
.
dgn-np:NP640747.RAShzmjVZV-sPN4E12DE56HSydGr9GhTfZ-9ezax9MB3c130_provenance
a
np:Provenance
.
dgn-np:NP640747.RAShzmjVZV-sPN4E12DE56HSydGr9GhTfZ-9ezax9MB3c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP640747.RAShzmjVZV-sPN4E12DE56HSydGr9GhTfZ-9ezax9MB3c130_assertion
{
miriam-gene:3605
a
ncit:C16612
.
lld:C0007847
a
ncit:C7057
.
dgn-gda:DGN4a3eb5a37802fa69b10f287e648a9e60
sio:SIO_000628
miriam-gene:3605
,
lld:C0007847
;
a
sio:SIO_001121
.
}
dgn-np:NP640747.RAShzmjVZV-sPN4E12DE56HSydGr9GhTfZ-9ezax9MB3c130_provenance
{
dgn-np:NP640747.RAShzmjVZV-sPN4E12DE56HSydGr9GhTfZ-9ezax9MB3c130_assertion
dcterms:description
"[Collectively, these findings suggested that IL17 gene polymorphism rs2275913 was associated with the susceptibility as well as positive peritumor intravascular cancer emboli and high clinical stage of cervical cancer in Chinese women.]. 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:23049595
;
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:NP640747.RAShzmjVZV-sPN4E12DE56HSydGr9GhTfZ-9ezax9MB3c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:26+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" .
}