@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP936194.RAhlUyRLQH8Oft72vNh59OvBTYKFfQUcOi1mdtb3orX8Y
> .
@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:NP936194.RAhlUyRLQH8Oft72vNh59OvBTYKFfQUcOi1mdtb3orX8Y130_head
{
this:
np:hasAssertion
dgn-np:NP936194.RAhlUyRLQH8Oft72vNh59OvBTYKFfQUcOi1mdtb3orX8Y130_assertion
;
np:hasProvenance
dgn-np:NP936194.RAhlUyRLQH8Oft72vNh59OvBTYKFfQUcOi1mdtb3orX8Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP936194.RAhlUyRLQH8Oft72vNh59OvBTYKFfQUcOi1mdtb3orX8Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP936194.RAhlUyRLQH8Oft72vNh59OvBTYKFfQUcOi1mdtb3orX8Y130_assertion
a
np:Assertion
.
dgn-np:NP936194.RAhlUyRLQH8Oft72vNh59OvBTYKFfQUcOi1mdtb3orX8Y130_provenance
a
np:Provenance
.
dgn-np:NP936194.RAhlUyRLQH8Oft72vNh59OvBTYKFfQUcOi1mdtb3orX8Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP936194.RAhlUyRLQH8Oft72vNh59OvBTYKFfQUcOi1mdtb3orX8Y130_assertion
{
miriam-gene:9211
a
ncit:C16612
.
lld:C0242363
a
ncit:C7057
.
dgn-gda:DGNa4a5f8ecc8a79dea9873c9c7f105db39
sio:SIO_000628
miriam-gene:9211
,
lld:C0242363
;
a
sio:SIO_001121
.
}
dgn-np:NP936194.RAhlUyRLQH8Oft72vNh59OvBTYKFfQUcOi1mdtb3orX8Y130_provenance
{
dgn-np:NP936194.RAhlUyRLQH8Oft72vNh59OvBTYKFfQUcOi1mdtb3orX8Y130_assertion
dcterms:description
"[We have studied 44 benign and malignant EPTs by comparative genomic hybridization to correlate the overall number of genetic alterations with clinical and histopathological parameters and to identify chromosomal regions which might harbor genes involved in EPT pathogenesis and progression.]. 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:10595906
;
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:NP936194.RAhlUyRLQH8Oft72vNh59OvBTYKFfQUcOi1mdtb3orX8Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:33+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" .
}