@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP695127.RA7NZhpzThsXa24pAGc5gDngFXh8j07iY65opjBzMXaPA
> .
@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:NP695127.RA7NZhpzThsXa24pAGc5gDngFXh8j07iY65opjBzMXaPA130_head
{
this:
np:hasAssertion
dgn-np:NP695127.RA7NZhpzThsXa24pAGc5gDngFXh8j07iY65opjBzMXaPA130_assertion
;
np:hasProvenance
dgn-np:NP695127.RA7NZhpzThsXa24pAGc5gDngFXh8j07iY65opjBzMXaPA130_provenance
;
np:hasPublicationInfo
dgn-np:NP695127.RA7NZhpzThsXa24pAGc5gDngFXh8j07iY65opjBzMXaPA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP695127.RA7NZhpzThsXa24pAGc5gDngFXh8j07iY65opjBzMXaPA130_assertion
a
np:Assertion
.
dgn-np:NP695127.RA7NZhpzThsXa24pAGc5gDngFXh8j07iY65opjBzMXaPA130_provenance
a
np:Provenance
.
dgn-np:NP695127.RA7NZhpzThsXa24pAGc5gDngFXh8j07iY65opjBzMXaPA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP695127.RA7NZhpzThsXa24pAGc5gDngFXh8j07iY65opjBzMXaPA130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0005695
a
ncit:C7057
.
dgn-gda:DGNd320a87dd2c1f05d004ba63939b7a1ed
sio:SIO_000628
miriam-gene:3342
,
lld:C0005695
;
a
sio:SIO_001121
.
}
dgn-np:NP695127.RA7NZhpzThsXa24pAGc5gDngFXh8j07iY65opjBzMXaPA130_provenance
{
dgn-np:NP695127.RA7NZhpzThsXa24pAGc5gDngFXh8j07iY65opjBzMXaPA130_assertion
dcterms:description
"[The aim of this study was to analyze the distribution of FGFR3 mutations in bladder tumors of different grade and stage and determine the relation of mutations to chromosomal alterations detected by comparative genomic hybridization (CGH).]. 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:18231634
;
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:NP695127.RA7NZhpzThsXa24pAGc5gDngFXh8j07iY65opjBzMXaPA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:03+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" .
}