@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP563490.RAFpA0A4OQBiqa2skmD20hcwPKSMiXmAa6kDf3I56KU0s
> .
@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:NP563490.RAFpA0A4OQBiqa2skmD20hcwPKSMiXmAa6kDf3I56KU0s130_head
{
this:
np:hasAssertion
dgn-np:NP563490.RAFpA0A4OQBiqa2skmD20hcwPKSMiXmAa6kDf3I56KU0s130_assertion
;
np:hasProvenance
dgn-np:NP563490.RAFpA0A4OQBiqa2skmD20hcwPKSMiXmAa6kDf3I56KU0s130_provenance
;
np:hasPublicationInfo
dgn-np:NP563490.RAFpA0A4OQBiqa2skmD20hcwPKSMiXmAa6kDf3I56KU0s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP563490.RAFpA0A4OQBiqa2skmD20hcwPKSMiXmAa6kDf3I56KU0s130_assertion
a
np:Assertion
.
dgn-np:NP563490.RAFpA0A4OQBiqa2skmD20hcwPKSMiXmAa6kDf3I56KU0s130_provenance
a
np:Provenance
.
dgn-np:NP563490.RAFpA0A4OQBiqa2skmD20hcwPKSMiXmAa6kDf3I56KU0s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP563490.RAFpA0A4OQBiqa2skmD20hcwPKSMiXmAa6kDf3I56KU0s130_assertion
{
miriam-gene:3725
a
ncit:C16612
.
lld:C0023827
a
ncit:C7057
.
dgn-gda:DGN17ad4569151911e91bcac7e09ce95ec3
sio:SIO_000628
miriam-gene:3725
,
lld:C0023827
;
a
sio:SIO_001121
.
}
dgn-np:NP563490.RAFpA0A4OQBiqa2skmD20hcwPKSMiXmAa6kDf3I56KU0s130_provenance
{
dgn-np:NP563490.RAFpA0A4OQBiqa2skmD20hcwPKSMiXmAa6kDf3I56KU0s130_assertion
dcterms:description
"[Of particular interest, amplicons containing genes involved in the c-jun NH2-terminal kinase/mitogen-activated protein kinase pathway, that is, JUN in 1p32 and MAP3K7IP2 (TAB2) in 6q24-25, were found to be independently amplified in eight of 11 cases with 12q amplification, providing strong support for the notion that aberrant expression of this pathway is an important step in the dedifferentiation of liposarcomas.]. 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:16732325
;
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:NP563490.RAFpA0A4OQBiqa2skmD20hcwPKSMiXmAa6kDf3I56KU0s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:39+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" .
}