@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP291702.RAV-NpExgUWvTLRR9bgmt9EnHPnlKkeRvJRBeIhtUPaTk
> .
@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:NP291702.RAV-NpExgUWvTLRR9bgmt9EnHPnlKkeRvJRBeIhtUPaTk130_head
{
this:
np:hasAssertion
dgn-np:NP291702.RAV-NpExgUWvTLRR9bgmt9EnHPnlKkeRvJRBeIhtUPaTk130_assertion
;
np:hasProvenance
dgn-np:NP291702.RAV-NpExgUWvTLRR9bgmt9EnHPnlKkeRvJRBeIhtUPaTk130_provenance
;
np:hasPublicationInfo
dgn-np:NP291702.RAV-NpExgUWvTLRR9bgmt9EnHPnlKkeRvJRBeIhtUPaTk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP291702.RAV-NpExgUWvTLRR9bgmt9EnHPnlKkeRvJRBeIhtUPaTk130_assertion
a
np:Assertion
.
dgn-np:NP291702.RAV-NpExgUWvTLRR9bgmt9EnHPnlKkeRvJRBeIhtUPaTk130_provenance
a
np:Provenance
.
dgn-np:NP291702.RAV-NpExgUWvTLRR9bgmt9EnHPnlKkeRvJRBeIhtUPaTk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP291702.RAV-NpExgUWvTLRR9bgmt9EnHPnlKkeRvJRBeIhtUPaTk130_assertion
{
miriam-gene:4255
a
ncit:C16612
.
lld:C0017636
a
ncit:C7057
.
dgn-gda:DGN37bb5a13d41422378bf6348d489f0d1a
sio:SIO_000628
miriam-gene:4255
,
lld:C0017636
;
a
sio:SIO_001121
.
}
dgn-np:NP291702.RAV-NpExgUWvTLRR9bgmt9EnHPnlKkeRvJRBeIhtUPaTk130_provenance
{
dgn-np:NP291702.RAV-NpExgUWvTLRR9bgmt9EnHPnlKkeRvJRBeIhtUPaTk130_assertion
dcterms:description
"[In fact, first steps have been undertaken in supplementing classical histopathological diagnosis by the use of molecular tests, such as MGMT promoter hypermethylation in glioblastomas or detection of losses of chromosome arms 1p and 19q in oligodendroglial tumors.]. 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:19333441
;
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:NP291702.RAV-NpExgUWvTLRR9bgmt9EnHPnlKkeRvJRBeIhtUPaTk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:46+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" .
}