@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP636338.RAPeoENXiI3ehmOCWA8iDmBcV-F8zIdz02XMfyV_z2cEg
> .
@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:NP636338.RAPeoENXiI3ehmOCWA8iDmBcV-F8zIdz02XMfyV_z2cEg130_head
{
this:
np:hasAssertion
dgn-np:NP636338.RAPeoENXiI3ehmOCWA8iDmBcV-F8zIdz02XMfyV_z2cEg130_assertion
;
np:hasProvenance
dgn-np:NP636338.RAPeoENXiI3ehmOCWA8iDmBcV-F8zIdz02XMfyV_z2cEg130_provenance
;
np:hasPublicationInfo
dgn-np:NP636338.RAPeoENXiI3ehmOCWA8iDmBcV-F8zIdz02XMfyV_z2cEg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP636338.RAPeoENXiI3ehmOCWA8iDmBcV-F8zIdz02XMfyV_z2cEg130_assertion
a
np:Assertion
.
dgn-np:NP636338.RAPeoENXiI3ehmOCWA8iDmBcV-F8zIdz02XMfyV_z2cEg130_provenance
a
np:Provenance
.
dgn-np:NP636338.RAPeoENXiI3ehmOCWA8iDmBcV-F8zIdz02XMfyV_z2cEg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP636338.RAPeoENXiI3ehmOCWA8iDmBcV-F8zIdz02XMfyV_z2cEg130_assertion
{
miriam-gene:6387
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGNf73ed54569d41a3ca49649557ab4b620
sio:SIO_000628
miriam-gene:6387
,
lld:C1527249
;
a
sio:SIO_001121
.
}
dgn-np:NP636338.RAPeoENXiI3ehmOCWA8iDmBcV-F8zIdz02XMfyV_z2cEg130_provenance
{
dgn-np:NP636338.RAPeoENXiI3ehmOCWA8iDmBcV-F8zIdz02XMfyV_z2cEg130_assertion
dcterms:description
"[Further studies with larger samples of patients are necessary to determine whether the CXCL12 polymorphism and plasma level reflect the clinical outcome of CRC and have an impact on CRC progression.]. 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:17143542
;
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:NP636338.RAPeoENXiI3ehmOCWA8iDmBcV-F8zIdz02XMfyV_z2cEg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:24+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" .
}