@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP893111.RAJT5661ID2R0BpqXeBAa5BZLSY_V6x04k_OIsD0xcHLE
> .
@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:NP893111.RAJT5661ID2R0BpqXeBAa5BZLSY_V6x04k_OIsD0xcHLE130_head
{
this:
np:hasAssertion
dgn-np:NP893111.RAJT5661ID2R0BpqXeBAa5BZLSY_V6x04k_OIsD0xcHLE130_assertion
;
np:hasProvenance
dgn-np:NP893111.RAJT5661ID2R0BpqXeBAa5BZLSY_V6x04k_OIsD0xcHLE130_provenance
;
np:hasPublicationInfo
dgn-np:NP893111.RAJT5661ID2R0BpqXeBAa5BZLSY_V6x04k_OIsD0xcHLE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP893111.RAJT5661ID2R0BpqXeBAa5BZLSY_V6x04k_OIsD0xcHLE130_assertion
a
np:Assertion
.
dgn-np:NP893111.RAJT5661ID2R0BpqXeBAa5BZLSY_V6x04k_OIsD0xcHLE130_provenance
a
np:Provenance
.
dgn-np:NP893111.RAJT5661ID2R0BpqXeBAa5BZLSY_V6x04k_OIsD0xcHLE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP893111.RAJT5661ID2R0BpqXeBAa5BZLSY_V6x04k_OIsD0xcHLE130_assertion
{
miriam-gene:8731
a
ncit:C16612
.
lld:C1457883
a
ncit:C7057
.
dgn-gda:DGN60d2008e909d9daa01149ecd52e5d396
sio:SIO_000628
miriam-gene:8731
,
lld:C1457883
;
a
sio:SIO_001121
.
}
dgn-np:NP893111.RAJT5661ID2R0BpqXeBAa5BZLSY_V6x04k_OIsD0xcHLE130_provenance
{
dgn-np:NP893111.RAJT5661ID2R0BpqXeBAa5BZLSY_V6x04k_OIsD0xcHLE130_assertion
dcterms:description
"[In primary myxofibrosarcomas, MET overexpression, as a frequent event, is likely driven by 7q gains with mRNA upregulation, associated with important prognosticators, and independently predictive of worse outcomes, highlighting its possible causative function in tumor aggressiveness and potentiality as a therapeutic target.]. 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:20639860
;
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:NP893111.RAJT5661ID2R0BpqXeBAa5BZLSY_V6x04k_OIsD0xcHLE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:09+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" .
}