@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP454935.RAZn1mBSwWiXfaf00oB7KcUuJd9fJrfsoCto9rnR3WDXI
> .
@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:NP454935.RAZn1mBSwWiXfaf00oB7KcUuJd9fJrfsoCto9rnR3WDXI130_head
{
this:
np:hasAssertion
dgn-np:NP454935.RAZn1mBSwWiXfaf00oB7KcUuJd9fJrfsoCto9rnR3WDXI130_assertion
;
np:hasProvenance
dgn-np:NP454935.RAZn1mBSwWiXfaf00oB7KcUuJd9fJrfsoCto9rnR3WDXI130_provenance
;
np:hasPublicationInfo
dgn-np:NP454935.RAZn1mBSwWiXfaf00oB7KcUuJd9fJrfsoCto9rnR3WDXI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP454935.RAZn1mBSwWiXfaf00oB7KcUuJd9fJrfsoCto9rnR3WDXI130_assertion
a
np:Assertion
.
dgn-np:NP454935.RAZn1mBSwWiXfaf00oB7KcUuJd9fJrfsoCto9rnR3WDXI130_provenance
a
np:Provenance
.
dgn-np:NP454935.RAZn1mBSwWiXfaf00oB7KcUuJd9fJrfsoCto9rnR3WDXI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP454935.RAZn1mBSwWiXfaf00oB7KcUuJd9fJrfsoCto9rnR3WDXI130_assertion
{
miriam-gene:27086
a
ncit:C16612
.
lld:C0024299
a
ncit:C7057
.
dgn-gda:DGNe5c3a1ec753c6bbd215fdafe2573c6a3
sio:SIO_000628
miriam-gene:27086
,
lld:C0024299
;
a
sio:SIO_001121
.
}
dgn-np:NP454935.RAZn1mBSwWiXfaf00oB7KcUuJd9fJrfsoCto9rnR3WDXI130_provenance
{
dgn-np:NP454935.RAZn1mBSwWiXfaf00oB7KcUuJd9fJrfsoCto9rnR3WDXI130_assertion
dcterms:description
"[Our findings suggest that (1) FOXP1 translocation may disrupt the full-length FOXP1 transcript and lead to expression of FOXP1 transcript variants with alternate 5' ends and (2) mechanisms other than translocation and copy number changes are also responsible for FOXP1 overexpression in lymphoma.]. 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:18487996
;
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:NP454935.RAZn1mBSwWiXfaf00oB7KcUuJd9fJrfsoCto9rnR3WDXI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:31+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" .
}