@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP477121.RATBn_JUiPqe-COcw5_RlPEXBMbPh5z_WuTW6RyZt8vkI
> .
@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:NP477121.RATBn_JUiPqe-COcw5_RlPEXBMbPh5z_WuTW6RyZt8vkI130_head
{
this:
np:hasAssertion
dgn-np:NP477121.RATBn_JUiPqe-COcw5_RlPEXBMbPh5z_WuTW6RyZt8vkI130_assertion
;
np:hasProvenance
dgn-np:NP477121.RATBn_JUiPqe-COcw5_RlPEXBMbPh5z_WuTW6RyZt8vkI130_provenance
;
np:hasPublicationInfo
dgn-np:NP477121.RATBn_JUiPqe-COcw5_RlPEXBMbPh5z_WuTW6RyZt8vkI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP477121.RATBn_JUiPqe-COcw5_RlPEXBMbPh5z_WuTW6RyZt8vkI130_assertion
a
np:Assertion
.
dgn-np:NP477121.RATBn_JUiPqe-COcw5_RlPEXBMbPh5z_WuTW6RyZt8vkI130_provenance
a
np:Provenance
.
dgn-np:NP477121.RATBn_JUiPqe-COcw5_RlPEXBMbPh5z_WuTW6RyZt8vkI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP477121.RATBn_JUiPqe-COcw5_RlPEXBMbPh5z_WuTW6RyZt8vkI130_assertion
{
miriam-gene:4582
a
ncit:C16612
.
lld:C0007134
a
ncit:C7057
.
dgn-gda:DGN0ceb72557207a8b0e9bf8364fd59bedc
sio:SIO_000628
miriam-gene:4582
,
lld:C0007134
;
a
sio:SIO_001121
.
}
dgn-np:NP477121.RATBn_JUiPqe-COcw5_RlPEXBMbPh5z_WuTW6RyZt8vkI130_provenance
{
dgn-np:NP477121.RATBn_JUiPqe-COcw5_RlPEXBMbPh5z_WuTW6RyZt8vkI130_assertion
dcterms:description
"[Xp11 translocation renal cell carcinoma (RCC) harbor various TFE3 gene fusions, and are known to underexpress epithelial immunohistochemical (IHC) markers such as cytokeratin and EMA relative to usual adult type RCC; however, their profile in reference to other IHC markers that are differentially expressed in other subtypes of RCC has not been systematically assessed.]. 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:20679884
;
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:NP477121.RATBn_JUiPqe-COcw5_RlPEXBMbPh5z_WuTW6RyZt8vkI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:45+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" .
}