@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP499332.RAvA3jKTIiJTgxlFnjN6BNvRIKz9nEJ2dIDgfK2ntHQ6c
> .
@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:NP499332.RAvA3jKTIiJTgxlFnjN6BNvRIKz9nEJ2dIDgfK2ntHQ6c130_head
{
this:
np:hasAssertion
dgn-np:NP499332.RAvA3jKTIiJTgxlFnjN6BNvRIKz9nEJ2dIDgfK2ntHQ6c130_assertion
;
np:hasProvenance
dgn-np:NP499332.RAvA3jKTIiJTgxlFnjN6BNvRIKz9nEJ2dIDgfK2ntHQ6c130_provenance
;
np:hasPublicationInfo
dgn-np:NP499332.RAvA3jKTIiJTgxlFnjN6BNvRIKz9nEJ2dIDgfK2ntHQ6c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP499332.RAvA3jKTIiJTgxlFnjN6BNvRIKz9nEJ2dIDgfK2ntHQ6c130_assertion
a
np:Assertion
.
dgn-np:NP499332.RAvA3jKTIiJTgxlFnjN6BNvRIKz9nEJ2dIDgfK2ntHQ6c130_provenance
a
np:Provenance
.
dgn-np:NP499332.RAvA3jKTIiJTgxlFnjN6BNvRIKz9nEJ2dIDgfK2ntHQ6c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP499332.RAvA3jKTIiJTgxlFnjN6BNvRIKz9nEJ2dIDgfK2ntHQ6c130_assertion
{
miriam-gene:6502
a
ncit:C16612
.
lld:C1333064
a
ncit:C7057
.
dgn-gda:DGN2efa07d33c63f8a6d514b38355edff1b
sio:SIO_000628
miriam-gene:6502
,
lld:C1333064
;
a
sio:SIO_001121
.
}
dgn-np:NP499332.RAvA3jKTIiJTgxlFnjN6BNvRIKz9nEJ2dIDgfK2ntHQ6c130_provenance
{
dgn-np:NP499332.RAvA3jKTIiJTgxlFnjN6BNvRIKz9nEJ2dIDgfK2ntHQ6c130_assertion
dcterms:description
"[In comparison to the germinal center profiles, the most frequent imbalances in HL were losses in 5p13 (AMACR, GDNF, and SKP2), and gains in 7q36 (SHH, sonic hedgehog homolog) and 9q34 (ABL1, CDK9, LCN2, and PTGES).]. 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:21385932
;
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:NP499332.RAvA3jKTIiJTgxlFnjN6BNvRIKz9nEJ2dIDgfK2ntHQ6c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:58+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" .
}