@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP324589.RANlJwrIRYbQjH4hFDu1pi1o8hje2_0FAORdMxdGNqqkk
> .
@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:NP324589.RANlJwrIRYbQjH4hFDu1pi1o8hje2_0FAORdMxdGNqqkk130_head
{
this:
np:hasAssertion
dgn-np:NP324589.RANlJwrIRYbQjH4hFDu1pi1o8hje2_0FAORdMxdGNqqkk130_assertion
;
np:hasProvenance
dgn-np:NP324589.RANlJwrIRYbQjH4hFDu1pi1o8hje2_0FAORdMxdGNqqkk130_provenance
;
np:hasPublicationInfo
dgn-np:NP324589.RANlJwrIRYbQjH4hFDu1pi1o8hje2_0FAORdMxdGNqqkk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP324589.RANlJwrIRYbQjH4hFDu1pi1o8hje2_0FAORdMxdGNqqkk130_assertion
a
np:Assertion
.
dgn-np:NP324589.RANlJwrIRYbQjH4hFDu1pi1o8hje2_0FAORdMxdGNqqkk130_provenance
a
np:Provenance
.
dgn-np:NP324589.RANlJwrIRYbQjH4hFDu1pi1o8hje2_0FAORdMxdGNqqkk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP324589.RANlJwrIRYbQjH4hFDu1pi1o8hje2_0FAORdMxdGNqqkk130_assertion
{
miriam-gene:1956
a
ncit:C16612
.
lld:C0004114
a
ncit:C7057
.
dgn-gda:DGN0b49e386b58b74496570825935f0d01c
sio:SIO_000628
miriam-gene:1956
,
lld:C0004114
;
a
sio:SIO_001121
.
}
dgn-np:NP324589.RANlJwrIRYbQjH4hFDu1pi1o8hje2_0FAORdMxdGNqqkk130_provenance
{
dgn-np:NP324589.RANlJwrIRYbQjH4hFDu1pi1o8hje2_0FAORdMxdGNqqkk130_assertion
dcterms:description
"[In addition, we have assessed the contribution of EGFR overexpression and amplification and LOH for chromosome 10, two genetic alterations commonly associated with the development of de novo adult glioblastoma for their roles in the development of de novo astrocytomas of childhood.]. 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:10764044
;
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:NP324589.RANlJwrIRYbQjH4hFDu1pi1o8hje2_0FAORdMxdGNqqkk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:10+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" .
}