@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP44004.RAdLlkiktTQtAr3TsF2BBvy0WYmmo0N021dPagWH9WbDY
> .
@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:NP44004.RAdLlkiktTQtAr3TsF2BBvy0WYmmo0N021dPagWH9WbDY130_head
{
this:
np:hasAssertion
dgn-np:NP44004.RAdLlkiktTQtAr3TsF2BBvy0WYmmo0N021dPagWH9WbDY130_assertion
;
np:hasProvenance
dgn-np:NP44004.RAdLlkiktTQtAr3TsF2BBvy0WYmmo0N021dPagWH9WbDY130_provenance
;
np:hasPublicationInfo
dgn-np:NP44004.RAdLlkiktTQtAr3TsF2BBvy0WYmmo0N021dPagWH9WbDY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP44004.RAdLlkiktTQtAr3TsF2BBvy0WYmmo0N021dPagWH9WbDY130_assertion
a
np:Assertion
.
dgn-np:NP44004.RAdLlkiktTQtAr3TsF2BBvy0WYmmo0N021dPagWH9WbDY130_provenance
a
np:Provenance
.
dgn-np:NP44004.RAdLlkiktTQtAr3TsF2BBvy0WYmmo0N021dPagWH9WbDY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP44004.RAdLlkiktTQtAr3TsF2BBvy0WYmmo0N021dPagWH9WbDY130_assertion
{
miriam-gene:2264
a
ncit:C16612
.
lld:C0376358
a
ncit:C7057
.
dgn-gda:DGN39b293fa23b5d82194b4a4c38e6baf73
sio:SIO_000628
miriam-gene:2264
,
lld:C0376358
;
a
sio:SIO_001122
.
}
dgn-np:NP44004.RAdLlkiktTQtAr3TsF2BBvy0WYmmo0N021dPagWH9WbDY130_provenance
{
dgn-np:NP44004.RAdLlkiktTQtAr3TsF2BBvy0WYmmo0N021dPagWH9WbDY130_assertion
dcterms:description
"[ The FGFR-4 Arg388 allele is associated with both an increased incidence and clinical aggressiveness of prostate cancer and results in changes in cellular motility and invasiveness in immortalized prostate epithelial cells consistent with the promotion of metastasis.]. 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:15448004
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP44004.RAdLlkiktTQtAr3TsF2BBvy0WYmmo0N021dPagWH9WbDY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:20+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" .
}