@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP264118.RA7NtcJHMMikXgTjgh55V_cb64IyP3-IVdSi6-GTEXBJ4
> .
@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:NP264118.RA7NtcJHMMikXgTjgh55V_cb64IyP3-IVdSi6-GTEXBJ4130_head
{
this:
np:hasAssertion
dgn-np:NP264118.RA7NtcJHMMikXgTjgh55V_cb64IyP3-IVdSi6-GTEXBJ4130_assertion
;
np:hasProvenance
dgn-np:NP264118.RA7NtcJHMMikXgTjgh55V_cb64IyP3-IVdSi6-GTEXBJ4130_provenance
;
np:hasPublicationInfo
dgn-np:NP264118.RA7NtcJHMMikXgTjgh55V_cb64IyP3-IVdSi6-GTEXBJ4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP264118.RA7NtcJHMMikXgTjgh55V_cb64IyP3-IVdSi6-GTEXBJ4130_assertion
a
np:Assertion
.
dgn-np:NP264118.RA7NtcJHMMikXgTjgh55V_cb64IyP3-IVdSi6-GTEXBJ4130_provenance
a
np:Provenance
.
dgn-np:NP264118.RA7NtcJHMMikXgTjgh55V_cb64IyP3-IVdSi6-GTEXBJ4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP264118.RA7NtcJHMMikXgTjgh55V_cb64IyP3-IVdSi6-GTEXBJ4130_assertion
{
miriam-gene:10664
a
ncit:C16612
.
lld:C0376358
a
ncit:C7057
.
dgn-gda:DGNbee220be05a1dc3f5bfe8e7ccdeb6ef7
sio:SIO_000628
miriam-gene:10664
,
lld:C0376358
;
a
sio:SIO_001121
.
}
dgn-np:NP264118.RA7NtcJHMMikXgTjgh55V_cb64IyP3-IVdSi6-GTEXBJ4130_provenance
{
dgn-np:NP264118.RA7NtcJHMMikXgTjgh55V_cb64IyP3-IVdSi6-GTEXBJ4130_assertion
dcterms:description
"[A widely expressed transcription factor with multiple DNA sequence specificity, CTCF, is localized at chromosome segment 16q22.1 within one of the smallest regions of overlap for common deletions in breast and prostate cancers.]. 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:9591631
;
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:NP264118.RA7NtcJHMMikXgTjgh55V_cb64IyP3-IVdSi6-GTEXBJ4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:27+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" .
}