@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP824218.RA9jLnDAfM9YrVDNPFUnfHKi8rBK9sORWVpRylyxqvIwc
> .
@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:NP824218.RA9jLnDAfM9YrVDNPFUnfHKi8rBK9sORWVpRylyxqvIwc130_head
{
this:
np:hasAssertion
dgn-np:NP824218.RA9jLnDAfM9YrVDNPFUnfHKi8rBK9sORWVpRylyxqvIwc130_assertion
;
np:hasProvenance
dgn-np:NP824218.RA9jLnDAfM9YrVDNPFUnfHKi8rBK9sORWVpRylyxqvIwc130_provenance
;
np:hasPublicationInfo
dgn-np:NP824218.RA9jLnDAfM9YrVDNPFUnfHKi8rBK9sORWVpRylyxqvIwc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP824218.RA9jLnDAfM9YrVDNPFUnfHKi8rBK9sORWVpRylyxqvIwc130_assertion
a
np:Assertion
.
dgn-np:NP824218.RA9jLnDAfM9YrVDNPFUnfHKi8rBK9sORWVpRylyxqvIwc130_provenance
a
np:Provenance
.
dgn-np:NP824218.RA9jLnDAfM9YrVDNPFUnfHKi8rBK9sORWVpRylyxqvIwc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP824218.RA9jLnDAfM9YrVDNPFUnfHKi8rBK9sORWVpRylyxqvIwc130_assertion
{
miriam-gene:9973
a
ncit:C16612
.
lld:C0025202
a
ncit:C7057
.
dgn-gda:DGNcb6f4b22f8ce2b6c0446037eb9d4c1ae
sio:SIO_000628
miriam-gene:9973
,
lld:C0025202
;
a
sio:SIO_001121
.
}
dgn-np:NP824218.RA9jLnDAfM9YrVDNPFUnfHKi8rBK9sORWVpRylyxqvIwc130_provenance
{
dgn-np:NP824218.RA9jLnDAfM9YrVDNPFUnfHKi8rBK9sORWVpRylyxqvIwc130_assertion
dcterms:description
"[We also demonstrate that although fusion oncogene expression in later stages of differentiation can transform mesenchymal progenitor cells and generate tumors resembling CCS generally, expression in cells retaining stem cell markers permits the full melanoma-related phenotype.]. 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:23410975
;
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:NP824218.RA9jLnDAfM9YrVDNPFUnfHKi8rBK9sORWVpRylyxqvIwc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:24+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" .
}