@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP191950.RAV2O702i4VkfTLY_s1siZ5b2CvmSb4PYfWmhNjxj3ZQA
> .
@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:NP191950.RAV2O702i4VkfTLY_s1siZ5b2CvmSb4PYfWmhNjxj3ZQA130_head
{
this:
np:hasAssertion
dgn-np:NP191950.RAV2O702i4VkfTLY_s1siZ5b2CvmSb4PYfWmhNjxj3ZQA130_assertion
;
np:hasProvenance
dgn-np:NP191950.RAV2O702i4VkfTLY_s1siZ5b2CvmSb4PYfWmhNjxj3ZQA130_provenance
;
np:hasPublicationInfo
dgn-np:NP191950.RAV2O702i4VkfTLY_s1siZ5b2CvmSb4PYfWmhNjxj3ZQA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP191950.RAV2O702i4VkfTLY_s1siZ5b2CvmSb4PYfWmhNjxj3ZQA130_assertion
a
np:Assertion
.
dgn-np:NP191950.RAV2O702i4VkfTLY_s1siZ5b2CvmSb4PYfWmhNjxj3ZQA130_provenance
a
np:Provenance
.
dgn-np:NP191950.RAV2O702i4VkfTLY_s1siZ5b2CvmSb4PYfWmhNjxj3ZQA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP191950.RAV2O702i4VkfTLY_s1siZ5b2CvmSb4PYfWmhNjxj3ZQA130_assertion
{
miriam-gene:2099
a
ncit:C16612
.
lld:C0007103
a
ncit:C7057
.
dgn-gda:DGN0626fba693bd41624ac3bd9620b03734
sio:SIO_000628
miriam-gene:2099
,
lld:C0007103
;
a
sio:SIO_001121
.
}
dgn-np:NP191950.RAV2O702i4VkfTLY_s1siZ5b2CvmSb4PYfWmhNjxj3ZQA130_provenance
{
dgn-np:NP191950.RAV2O702i4VkfTLY_s1siZ5b2CvmSb4PYfWmhNjxj3ZQA130_assertion
dcterms:description
"[As few studies examine concurrent CXCL12, CXCR4, and estrogen receptor (ER) expression in EC patients, we examined this pathway in 199 EC patients with data from the University of Pittsburgh Medical Center Cancer Registry.]. 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:22025313
;
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:NP191950.RAV2O702i4VkfTLY_s1siZ5b2CvmSb4PYfWmhNjxj3ZQA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:45+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" .
}