@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP889618.RAlNCUiPIif3fE5537U0YCziLF2xWrCm29DaUnyYcYmd4
> .
@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:NP889618.RAlNCUiPIif3fE5537U0YCziLF2xWrCm29DaUnyYcYmd4130_head
{
this:
np:hasAssertion
dgn-np:NP889618.RAlNCUiPIif3fE5537U0YCziLF2xWrCm29DaUnyYcYmd4130_assertion
;
np:hasProvenance
dgn-np:NP889618.RAlNCUiPIif3fE5537U0YCziLF2xWrCm29DaUnyYcYmd4130_provenance
;
np:hasPublicationInfo
dgn-np:NP889618.RAlNCUiPIif3fE5537U0YCziLF2xWrCm29DaUnyYcYmd4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP889618.RAlNCUiPIif3fE5537U0YCziLF2xWrCm29DaUnyYcYmd4130_assertion
a
np:Assertion
.
dgn-np:NP889618.RAlNCUiPIif3fE5537U0YCziLF2xWrCm29DaUnyYcYmd4130_provenance
a
np:Provenance
.
dgn-np:NP889618.RAlNCUiPIif3fE5537U0YCziLF2xWrCm29DaUnyYcYmd4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP889618.RAlNCUiPIif3fE5537U0YCziLF2xWrCm29DaUnyYcYmd4130_assertion
{
miriam-gene:1719
a
ncit:C16612
.
lld:C0029463
a
ncit:C7057
.
dgn-gda:DGN5336da1f420845c99e8d6e02b1575911
sio:SIO_000628
miriam-gene:1719
,
lld:C0029463
;
a
sio:SIO_001121
.
}
dgn-np:NP889618.RAlNCUiPIif3fE5537U0YCziLF2xWrCm29DaUnyYcYmd4130_provenance
{
dgn-np:NP889618.RAlNCUiPIif3fE5537U0YCziLF2xWrCm29DaUnyYcYmd4130_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:NP889618.RAlNCUiPIif3fE5537U0YCziLF2xWrCm29DaUnyYcYmd4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:07+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" .
}