@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP173074.RAfbFsPoqMectLV_5dmx8s_IGSWzBl7Z3UchOAfQoWjmQ
> .
@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:NP173074.RAfbFsPoqMectLV_5dmx8s_IGSWzBl7Z3UchOAfQoWjmQ130_head
{
this:
np:hasAssertion
dgn-np:NP173074.RAfbFsPoqMectLV_5dmx8s_IGSWzBl7Z3UchOAfQoWjmQ130_assertion
;
np:hasProvenance
dgn-np:NP173074.RAfbFsPoqMectLV_5dmx8s_IGSWzBl7Z3UchOAfQoWjmQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP173074.RAfbFsPoqMectLV_5dmx8s_IGSWzBl7Z3UchOAfQoWjmQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP173074.RAfbFsPoqMectLV_5dmx8s_IGSWzBl7Z3UchOAfQoWjmQ130_assertion
a
np:Assertion
.
dgn-np:NP173074.RAfbFsPoqMectLV_5dmx8s_IGSWzBl7Z3UchOAfQoWjmQ130_provenance
a
np:Provenance
.
dgn-np:NP173074.RAfbFsPoqMectLV_5dmx8s_IGSWzBl7Z3UchOAfQoWjmQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP173074.RAfbFsPoqMectLV_5dmx8s_IGSWzBl7Z3UchOAfQoWjmQ130_assertion
{
miriam-gene:8842
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGNb40d6c6e52f12086986626ec2ba7db9d
sio:SIO_000628
miriam-gene:8842
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP173074.RAfbFsPoqMectLV_5dmx8s_IGSWzBl7Z3UchOAfQoWjmQ130_provenance
{
dgn-np:NP173074.RAfbFsPoqMectLV_5dmx8s_IGSWzBl7Z3UchOAfQoWjmQ130_assertion
dcterms:description
"[More importantly, the CD133 gene signature identifies an aggressive subtype of GBM seen in younger patients with shorter survival who bear excessive genomic mutations as surveyed through the Cancer Genome Atlas Network GBM mutation spectrum.]. 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:21220328
;
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:NP173074.RAfbFsPoqMectLV_5dmx8s_IGSWzBl7Z3UchOAfQoWjmQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:33+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" .
}