@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP163896.RAp4E3AVEkypOMOAeUHgS5Z2r4nOao9aowQes19cZjXaU
> .
@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:NP163896.RAp4E3AVEkypOMOAeUHgS5Z2r4nOao9aowQes19cZjXaU130_head
{
this:
np:hasAssertion
dgn-np:NP163896.RAp4E3AVEkypOMOAeUHgS5Z2r4nOao9aowQes19cZjXaU130_assertion
;
np:hasProvenance
dgn-np:NP163896.RAp4E3AVEkypOMOAeUHgS5Z2r4nOao9aowQes19cZjXaU130_provenance
;
np:hasPublicationInfo
dgn-np:NP163896.RAp4E3AVEkypOMOAeUHgS5Z2r4nOao9aowQes19cZjXaU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP163896.RAp4E3AVEkypOMOAeUHgS5Z2r4nOao9aowQes19cZjXaU130_assertion
a
np:Assertion
.
dgn-np:NP163896.RAp4E3AVEkypOMOAeUHgS5Z2r4nOao9aowQes19cZjXaU130_provenance
a
np:Provenance
.
dgn-np:NP163896.RAp4E3AVEkypOMOAeUHgS5Z2r4nOao9aowQes19cZjXaU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP163896.RAp4E3AVEkypOMOAeUHgS5Z2r4nOao9aowQes19cZjXaU130_assertion
{
miriam-gene:4255
a
ncit:C16612
.
lld:C0751396
a
ncit:C7057
.
dgn-gda:DGN7a54fa0281b76730294e46215f4ed33b
sio:SIO_000628
miriam-gene:4255
,
lld:C0751396
;
a
sio:SIO_001121
.
}
dgn-np:NP163896.RAp4E3AVEkypOMOAeUHgS5Z2r4nOao9aowQes19cZjXaU130_provenance
{
dgn-np:NP163896.RAp4E3AVEkypOMOAeUHgS5Z2r4nOao9aowQes19cZjXaU130_assertion
dcterms:description
"[The relationship between chromosome 1p and 19q deletions and treatment responsive oligodendrogliomas is discussed, as are the newer advances relating to silencing of the MGMT gene in astrocytomas and mutations in the IDH-1 gene in both astrocytomas and oligodendrogliomas.]. 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:21233669
;
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:NP163896.RAp4E3AVEkypOMOAeUHgS5Z2r4nOao9aowQes19cZjXaU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:28+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" .
}