@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP420200.RA6b2QYsEVbJaxMkfpAZtsK__1XhhwoAo7sh1Yl8qwX6k
> .
@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:NP420200.RA6b2QYsEVbJaxMkfpAZtsK__1XhhwoAo7sh1Yl8qwX6k130_head
{
this:
np:hasAssertion
dgn-np:NP420200.RA6b2QYsEVbJaxMkfpAZtsK__1XhhwoAo7sh1Yl8qwX6k130_assertion
;
np:hasProvenance
dgn-np:NP420200.RA6b2QYsEVbJaxMkfpAZtsK__1XhhwoAo7sh1Yl8qwX6k130_provenance
;
np:hasPublicationInfo
dgn-np:NP420200.RA6b2QYsEVbJaxMkfpAZtsK__1XhhwoAo7sh1Yl8qwX6k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP420200.RA6b2QYsEVbJaxMkfpAZtsK__1XhhwoAo7sh1Yl8qwX6k130_assertion
a
np:Assertion
.
dgn-np:NP420200.RA6b2QYsEVbJaxMkfpAZtsK__1XhhwoAo7sh1Yl8qwX6k130_provenance
a
np:Provenance
.
dgn-np:NP420200.RA6b2QYsEVbJaxMkfpAZtsK__1XhhwoAo7sh1Yl8qwX6k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP420200.RA6b2QYsEVbJaxMkfpAZtsK__1XhhwoAo7sh1Yl8qwX6k130_assertion
{
miriam-gene:8091
a
ncit:C16612
.
lld:C1306242
a
ncit:C7057
.
dgn-gda:DGNcb45b54ce14ffae6a59173f504901b96
sio:SIO_000628
miriam-gene:8091
,
lld:C1306242
;
a
sio:SIO_001121
.
}
dgn-np:NP420200.RA6b2QYsEVbJaxMkfpAZtsK__1XhhwoAo7sh1Yl8qwX6k130_provenance
{
dgn-np:NP420200.RA6b2QYsEVbJaxMkfpAZtsK__1XhhwoAo7sh1Yl8qwX6k130_assertion
dcterms:description
"[To shed more light on the pathobiology of aggressive angiomyxoma and to investigate the molecular mechanisms behind the involvement of the HMGA2 gene in this tumor type (fusion transcript vs deregulated expression), we investigated, cytogenetically and with molecular techniques, one such tumor which presented a t(11;12)(q23;q15) as the sole karyotypic aberration.]. 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:16568309
;
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:NP420200.RA6b2QYsEVbJaxMkfpAZtsK__1XhhwoAo7sh1Yl8qwX6k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:09+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" .
}