@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP617352.RAITmpwWzNz6ofobLFQ68KhkQL-iDYAWV8OkHC2b8LidE
> .
@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:NP617352.RAITmpwWzNz6ofobLFQ68KhkQL-iDYAWV8OkHC2b8LidE130_head
{
this:
np:hasAssertion
dgn-np:NP617352.RAITmpwWzNz6ofobLFQ68KhkQL-iDYAWV8OkHC2b8LidE130_assertion
;
np:hasProvenance
dgn-np:NP617352.RAITmpwWzNz6ofobLFQ68KhkQL-iDYAWV8OkHC2b8LidE130_provenance
;
np:hasPublicationInfo
dgn-np:NP617352.RAITmpwWzNz6ofobLFQ68KhkQL-iDYAWV8OkHC2b8LidE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP617352.RAITmpwWzNz6ofobLFQ68KhkQL-iDYAWV8OkHC2b8LidE130_assertion
a
np:Assertion
.
dgn-np:NP617352.RAITmpwWzNz6ofobLFQ68KhkQL-iDYAWV8OkHC2b8LidE130_provenance
a
np:Provenance
.
dgn-np:NP617352.RAITmpwWzNz6ofobLFQ68KhkQL-iDYAWV8OkHC2b8LidE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP617352.RAITmpwWzNz6ofobLFQ68KhkQL-iDYAWV8OkHC2b8LidE130_assertion
{
miriam-gene:53373
a
ncit:C16612
.
lld:C0238463
a
ncit:C7057
.
dgn-gda:DGNfdff901226bf7fa55e4ebc207232f1db
sio:SIO_000628
miriam-gene:53373
,
lld:C0238463
;
a
sio:SIO_001121
.
}
dgn-np:NP617352.RAITmpwWzNz6ofobLFQ68KhkQL-iDYAWV8OkHC2b8LidE130_provenance
{
dgn-np:NP617352.RAITmpwWzNz6ofobLFQ68KhkQL-iDYAWV8OkHC2b8LidE130_assertion
dcterms:description
"[In 3 thyroid cancer cell lines (TPC1 from a papillary thyroid cancer, FTC133 from a follicular thyroid cancer, XTC1 from a Hürthle cell carcinoma), small interfering RNA knockdown of RTN4IP1 was used to determine its role in regulating the hallmarks of malignant cell phenotype (cellular proliferation, migration, apoptosis, invasion, tumor spheroid formation, anchorage independent growth).]. 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:23393170
;
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:NP617352.RAITmpwWzNz6ofobLFQ68KhkQL-iDYAWV8OkHC2b8LidE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:13+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" .
}