@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP738563.RAI_gY8YmTO9QDV1ej3xM379MuK8mP_JFuWI8gn5oaFKA
> .
@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:NP738563.RAI_gY8YmTO9QDV1ej3xM379MuK8mP_JFuWI8gn5oaFKA130_head
{
this:
np:hasAssertion
dgn-np:NP738563.RAI_gY8YmTO9QDV1ej3xM379MuK8mP_JFuWI8gn5oaFKA130_assertion
;
np:hasProvenance
dgn-np:NP738563.RAI_gY8YmTO9QDV1ej3xM379MuK8mP_JFuWI8gn5oaFKA130_provenance
;
np:hasPublicationInfo
dgn-np:NP738563.RAI_gY8YmTO9QDV1ej3xM379MuK8mP_JFuWI8gn5oaFKA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP738563.RAI_gY8YmTO9QDV1ej3xM379MuK8mP_JFuWI8gn5oaFKA130_assertion
a
np:Assertion
.
dgn-np:NP738563.RAI_gY8YmTO9QDV1ej3xM379MuK8mP_JFuWI8gn5oaFKA130_provenance
a
np:Provenance
.
dgn-np:NP738563.RAI_gY8YmTO9QDV1ej3xM379MuK8mP_JFuWI8gn5oaFKA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP738563.RAI_gY8YmTO9QDV1ej3xM379MuK8mP_JFuWI8gn5oaFKA130_assertion
{
miriam-gene:4856
a
ncit:C16612
.
lld:C0684337
a
ncit:C7057
.
dgn-gda:DGNcbe2b9fcf233e1dda1f6ed36a342b400
sio:SIO_000628
miriam-gene:4856
,
lld:C0684337
;
a
sio:SIO_001121
.
}
dgn-np:NP738563.RAI_gY8YmTO9QDV1ej3xM379MuK8mP_JFuWI8gn5oaFKA130_provenance
{
dgn-np:NP738563.RAI_gY8YmTO9QDV1ej3xM379MuK8mP_JFuWI8gn5oaFKA130_assertion
dcterms:description
"[Polyclonal antibodies directed against each of the different CCN3 modules were used to identify variant CCN3 proteins in tumors and to draw potential relationships between the expression of these variants and the outcome of patients with Ewing sarcoma.]. 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:19695675
;
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:NP738563.RAI_gY8YmTO9QDV1ej3xM379MuK8mP_JFuWI8gn5oaFKA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:28+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" .
}