@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP608298.RAE9N8YrA-dbd9Lw9v56Ia7xf27bThEI6r_YmM0fyeyLo
> .
@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:NP608298.RAE9N8YrA-dbd9Lw9v56Ia7xf27bThEI6r_YmM0fyeyLo130_head
{
this:
np:hasAssertion
dgn-np:NP608298.RAE9N8YrA-dbd9Lw9v56Ia7xf27bThEI6r_YmM0fyeyLo130_assertion
;
np:hasProvenance
dgn-np:NP608298.RAE9N8YrA-dbd9Lw9v56Ia7xf27bThEI6r_YmM0fyeyLo130_provenance
;
np:hasPublicationInfo
dgn-np:NP608298.RAE9N8YrA-dbd9Lw9v56Ia7xf27bThEI6r_YmM0fyeyLo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP608298.RAE9N8YrA-dbd9Lw9v56Ia7xf27bThEI6r_YmM0fyeyLo130_assertion
a
np:Assertion
.
dgn-np:NP608298.RAE9N8YrA-dbd9Lw9v56Ia7xf27bThEI6r_YmM0fyeyLo130_provenance
a
np:Provenance
.
dgn-np:NP608298.RAE9N8YrA-dbd9Lw9v56Ia7xf27bThEI6r_YmM0fyeyLo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP608298.RAE9N8YrA-dbd9Lw9v56Ia7xf27bThEI6r_YmM0fyeyLo130_assertion
{
miriam-gene:1029
a
ncit:C16612
.
lld:C0206663
a
ncit:C7057
.
dgn-gda:DGN9588e77eca2ff5041a7ed2bdf074ee9b
sio:SIO_000628
miriam-gene:1029
,
lld:C0206663
;
a
sio:SIO_001121
.
}
dgn-np:NP608298.RAE9N8YrA-dbd9Lw9v56Ia7xf27bThEI6r_YmM0fyeyLo130_provenance
{
dgn-np:NP608298.RAE9N8YrA-dbd9Lw9v56Ia7xf27bThEI6r_YmM0fyeyLo130_assertion
dcterms:description
"[In this study the authors have examined DNA from 20 primary PNETs in children and from 20 malignant astrocytomas to assess the frequency of P16ink4 and CDK4 gene alterations associated with each type of tumor.]. 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:8847566
;
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:NP608298.RAE9N8YrA-dbd9Lw9v56Ia7xf27bThEI6r_YmM0fyeyLo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:05+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" .
}