@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP228749.RA17mbgyJGkyVGANIUtWYSWDY9FPw1YU3gxuNbRkFTRyw
> .
@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:NP228749.RA17mbgyJGkyVGANIUtWYSWDY9FPw1YU3gxuNbRkFTRyw130_head
{
this:
np:hasAssertion
dgn-np:NP228749.RA17mbgyJGkyVGANIUtWYSWDY9FPw1YU3gxuNbRkFTRyw130_assertion
;
np:hasProvenance
dgn-np:NP228749.RA17mbgyJGkyVGANIUtWYSWDY9FPw1YU3gxuNbRkFTRyw130_provenance
;
np:hasPublicationInfo
dgn-np:NP228749.RA17mbgyJGkyVGANIUtWYSWDY9FPw1YU3gxuNbRkFTRyw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP228749.RA17mbgyJGkyVGANIUtWYSWDY9FPw1YU3gxuNbRkFTRyw130_assertion
a
np:Assertion
.
dgn-np:NP228749.RA17mbgyJGkyVGANIUtWYSWDY9FPw1YU3gxuNbRkFTRyw130_provenance
a
np:Provenance
.
dgn-np:NP228749.RA17mbgyJGkyVGANIUtWYSWDY9FPw1YU3gxuNbRkFTRyw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP228749.RA17mbgyJGkyVGANIUtWYSWDY9FPw1YU3gxuNbRkFTRyw130_assertion
{
miriam-gene:5670
a
ncit:C16612
.
lld:C0686619
a
ncit:C7057
.
dgn-gda:DGN72b0ad3ad1e50758cb6ee9464d293f16
sio:SIO_000628
miriam-gene:5670
,
lld:C0686619
;
a
sio:SIO_001121
.
}
dgn-np:NP228749.RA17mbgyJGkyVGANIUtWYSWDY9FPw1YU3gxuNbRkFTRyw130_provenance
{
dgn-np:NP228749.RA17mbgyJGkyVGANIUtWYSWDY9FPw1YU3gxuNbRkFTRyw130_assertion
dcterms:description
"[Univariate analyses showed that lower OS and DFS rates were significantly associated with GCC and CK20 mRNA levels, the presence of lymph node metastases, the presence of mesenteric root lymph node metastases, and the presence of tumor emboli in vessels (p < 0.05), but not with CEA levels.]. 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:23150200
;
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:NP228749.RA17mbgyJGkyVGANIUtWYSWDY9FPw1YU3gxuNbRkFTRyw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:08+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" .
}