@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP564270.RA1aL3tGEX1Zf2gRM_iGGL26juyCi86n6VEO0bMtUN3nw
> .
@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:NP564270.RA1aL3tGEX1Zf2gRM_iGGL26juyCi86n6VEO0bMtUN3nw130_head
{
this:
np:hasAssertion
dgn-np:NP564270.RA1aL3tGEX1Zf2gRM_iGGL26juyCi86n6VEO0bMtUN3nw130_assertion
;
np:hasProvenance
dgn-np:NP564270.RA1aL3tGEX1Zf2gRM_iGGL26juyCi86n6VEO0bMtUN3nw130_provenance
;
np:hasPublicationInfo
dgn-np:NP564270.RA1aL3tGEX1Zf2gRM_iGGL26juyCi86n6VEO0bMtUN3nw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP564270.RA1aL3tGEX1Zf2gRM_iGGL26juyCi86n6VEO0bMtUN3nw130_assertion
a
np:Assertion
.
dgn-np:NP564270.RA1aL3tGEX1Zf2gRM_iGGL26juyCi86n6VEO0bMtUN3nw130_provenance
a
np:Provenance
.
dgn-np:NP564270.RA1aL3tGEX1Zf2gRM_iGGL26juyCi86n6VEO0bMtUN3nw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP564270.RA1aL3tGEX1Zf2gRM_iGGL26juyCi86n6VEO0bMtUN3nw130_assertion
{
miriam-gene:2064
a
ncit:C16612
.
lld:C0205697
a
ncit:C7057
.
dgn-gda:DGN8404d902fd2471cec1a1640020e361ed
sio:SIO_000628
miriam-gene:2064
,
lld:C0205697
;
a
sio:SIO_001121
.
}
dgn-np:NP564270.RA1aL3tGEX1Zf2gRM_iGGL26juyCi86n6VEO0bMtUN3nw130_provenance
{
dgn-np:NP564270.RA1aL3tGEX1Zf2gRM_iGGL26juyCi86n6VEO0bMtUN3nw130_assertion
dcterms:description
"[The components of a biphasic spindle cell carcinoma harboured similar gains, losses, amplifications of 9p23 and 17q12 (HER2) and identical TP53 mutations, suggesting that these were relatively early events in the development of this tumour; however, each component displayed divergent focal amplifications.]. 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:20099298
;
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:NP564270.RA1aL3tGEX1Zf2gRM_iGGL26juyCi86n6VEO0bMtUN3nw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:40+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" .
}