@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP897487.RAzisNLHCQ0pPAHDtM5baC88-XKjNM830WZZxXgprvjRw
> .
@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:NP897487.RAzisNLHCQ0pPAHDtM5baC88-XKjNM830WZZxXgprvjRw130_head
{
this:
np:hasAssertion
dgn-np:NP897487.RAzisNLHCQ0pPAHDtM5baC88-XKjNM830WZZxXgprvjRw130_assertion
;
np:hasProvenance
dgn-np:NP897487.RAzisNLHCQ0pPAHDtM5baC88-XKjNM830WZZxXgprvjRw130_provenance
;
np:hasPublicationInfo
dgn-np:NP897487.RAzisNLHCQ0pPAHDtM5baC88-XKjNM830WZZxXgprvjRw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP897487.RAzisNLHCQ0pPAHDtM5baC88-XKjNM830WZZxXgprvjRw130_assertion
a
np:Assertion
.
dgn-np:NP897487.RAzisNLHCQ0pPAHDtM5baC88-XKjNM830WZZxXgprvjRw130_provenance
a
np:Provenance
.
dgn-np:NP897487.RAzisNLHCQ0pPAHDtM5baC88-XKjNM830WZZxXgprvjRw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP897487.RAzisNLHCQ0pPAHDtM5baC88-XKjNM830WZZxXgprvjRw130_assertion
{
miriam-gene:4609
a
ncit:C16612
.
lld:C0029463
a
ncit:C7057
.
dgn-gda:DGNa83c98fc60001e066d3460308ee2773f
sio:SIO_000628
miriam-gene:4609
,
lld:C0029463
;
a
sio:SIO_001121
.
}
dgn-np:NP897487.RAzisNLHCQ0pPAHDtM5baC88-XKjNM830WZZxXgprvjRw130_provenance
{
dgn-np:NP897487.RAzisNLHCQ0pPAHDtM5baC88-XKjNM830WZZxXgprvjRw130_assertion
dcterms:description
"[The assessment of C-MYC and DHFR at diagnosis, together with that of other known prognostic markers, can be considered for an early identification of subgroups of OS patients with higher risk of adverse outcome.]. 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:18385200
;
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:NP897487.RAzisNLHCQ0pPAHDtM5baC88-XKjNM830WZZxXgprvjRw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:11+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" .
}