@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP373393.RAENn5xfvc_gXbNAGjAFYeAnrzy7nBlTVbvYygn8lc98Y
> .
@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:NP373393.RAENn5xfvc_gXbNAGjAFYeAnrzy7nBlTVbvYygn8lc98Y130_head
{
this:
np:hasAssertion
dgn-np:NP373393.RAENn5xfvc_gXbNAGjAFYeAnrzy7nBlTVbvYygn8lc98Y130_assertion
;
np:hasProvenance
dgn-np:NP373393.RAENn5xfvc_gXbNAGjAFYeAnrzy7nBlTVbvYygn8lc98Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP373393.RAENn5xfvc_gXbNAGjAFYeAnrzy7nBlTVbvYygn8lc98Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP373393.RAENn5xfvc_gXbNAGjAFYeAnrzy7nBlTVbvYygn8lc98Y130_assertion
a
np:Assertion
.
dgn-np:NP373393.RAENn5xfvc_gXbNAGjAFYeAnrzy7nBlTVbvYygn8lc98Y130_provenance
a
np:Provenance
.
dgn-np:NP373393.RAENn5xfvc_gXbNAGjAFYeAnrzy7nBlTVbvYygn8lc98Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP373393.RAENn5xfvc_gXbNAGjAFYeAnrzy7nBlTVbvYygn8lc98Y130_assertion
{
miriam-gene:7301
a
ncit:C16612
.
lld:C0007137
a
ncit:C7057
.
dgn-gda:DGNe0033c42af5f618696a5f33b04bd36e5
sio:SIO_000628
miriam-gene:7301
,
lld:C0007137
;
a
sio:SIO_001121
.
}
dgn-np:NP373393.RAENn5xfvc_gXbNAGjAFYeAnrzy7nBlTVbvYygn8lc98Y130_provenance
{
dgn-np:NP373393.RAENn5xfvc_gXbNAGjAFYeAnrzy7nBlTVbvYygn8lc98Y130_assertion
dcterms:description
"[We investigated relationships between DNA copy number aberrations and chromosomal structural rearrangements in 11 different cell lines derived from oral squamous cell carcinoma (OSCC) by comparative genomic hybridization (CGH), spectral karyotyping (SKY), and fluorescence in situ hybridization (FISH).]. 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:16737909
;
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:NP373393.RAENn5xfvc_gXbNAGjAFYeAnrzy7nBlTVbvYygn8lc98Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:38+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" .
}