@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP425794.RAR4eoYktBV-TtCx3gRrcadGRIB1IdERDKC91vwRuV_Po
> .
@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:NP425794.RAR4eoYktBV-TtCx3gRrcadGRIB1IdERDKC91vwRuV_Po130_head
{
this:
np:hasAssertion
dgn-np:NP425794.RAR4eoYktBV-TtCx3gRrcadGRIB1IdERDKC91vwRuV_Po130_assertion
;
np:hasProvenance
dgn-np:NP425794.RAR4eoYktBV-TtCx3gRrcadGRIB1IdERDKC91vwRuV_Po130_provenance
;
np:hasPublicationInfo
dgn-np:NP425794.RAR4eoYktBV-TtCx3gRrcadGRIB1IdERDKC91vwRuV_Po130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP425794.RAR4eoYktBV-TtCx3gRrcadGRIB1IdERDKC91vwRuV_Po130_assertion
a
np:Assertion
.
dgn-np:NP425794.RAR4eoYktBV-TtCx3gRrcadGRIB1IdERDKC91vwRuV_Po130_provenance
a
np:Provenance
.
dgn-np:NP425794.RAR4eoYktBV-TtCx3gRrcadGRIB1IdERDKC91vwRuV_Po130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP425794.RAR4eoYktBV-TtCx3gRrcadGRIB1IdERDKC91vwRuV_Po130_assertion
{
miriam-gene:1894
a
ncit:C16612
.
lld:C0009402
a
ncit:C7057
.
dgn-gda:DGNec3069a31c0954981f3acfc199dc4ffe
sio:SIO_000628
miriam-gene:1894
,
lld:C0009402
;
a
sio:SIO_001121
.
}
dgn-np:NP425794.RAR4eoYktBV-TtCx3gRrcadGRIB1IdERDKC91vwRuV_Po130_provenance
{
dgn-np:NP425794.RAR4eoYktBV-TtCx3gRrcadGRIB1IdERDKC91vwRuV_Po130_assertion
dcterms:description
"[Furthermore, high-level expression of RPS4X was associated with nonmucinous cancer cell type and that of ECT2 with lack of lymphatic invasion while upregulation of CKS2 was correlated with early tumor stage and lack of family history of CRC.]. 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:21304002
;
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:NP425794.RAR4eoYktBV-TtCx3gRrcadGRIB1IdERDKC91vwRuV_Po130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:12+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" .
}