@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP723698.RALnLQ8wBIPcSYDazIElTFDdRVtjMt8ZRXUG3_PNLG3lk
> .
@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:NP723698.RALnLQ8wBIPcSYDazIElTFDdRVtjMt8ZRXUG3_PNLG3lk130_head
{
this:
np:hasAssertion
dgn-np:NP723698.RALnLQ8wBIPcSYDazIElTFDdRVtjMt8ZRXUG3_PNLG3lk130_assertion
;
np:hasProvenance
dgn-np:NP723698.RALnLQ8wBIPcSYDazIElTFDdRVtjMt8ZRXUG3_PNLG3lk130_provenance
;
np:hasPublicationInfo
dgn-np:NP723698.RALnLQ8wBIPcSYDazIElTFDdRVtjMt8ZRXUG3_PNLG3lk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP723698.RALnLQ8wBIPcSYDazIElTFDdRVtjMt8ZRXUG3_PNLG3lk130_assertion
a
np:Assertion
.
dgn-np:NP723698.RALnLQ8wBIPcSYDazIElTFDdRVtjMt8ZRXUG3_PNLG3lk130_provenance
a
np:Provenance
.
dgn-np:NP723698.RALnLQ8wBIPcSYDazIElTFDdRVtjMt8ZRXUG3_PNLG3lk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP723698.RALnLQ8wBIPcSYDazIElTFDdRVtjMt8ZRXUG3_PNLG3lk130_assertion
{
miriam-gene:7030
a
ncit:C16612
.
lld:C3160732
a
ncit:C7057
.
dgn-gda:DGNe7ddc60678a7c08764b589007e54c85a
sio:SIO_000628
miriam-gene:7030
,
lld:C3160732
;
a
sio:SIO_001121
.
}
dgn-np:NP723698.RALnLQ8wBIPcSYDazIElTFDdRVtjMt8ZRXUG3_PNLG3lk130_provenance
{
dgn-np:NP723698.RALnLQ8wBIPcSYDazIElTFDdRVtjMt8ZRXUG3_PNLG3lk130_assertion
dcterms:description
"[The consistent immunohistochemical staining for TFE3 in all RCC with unusual histology, regardless of patient age, is likely to expand the spectrum of Xp11.2 translocation RCC with respect to age, clinical behavior, and molecular abnormalities.]. 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:20073616
;
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:NP723698.RALnLQ8wBIPcSYDazIElTFDdRVtjMt8ZRXUG3_PNLG3lk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:19+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" .
}