@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP495118.RAN3yrA7oSyE6EG1mvCcfPrbFBLeJrXCBaYDes397ZkRA
> .
@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:NP495118.RAN3yrA7oSyE6EG1mvCcfPrbFBLeJrXCBaYDes397ZkRA130_head
{
this:
np:hasAssertion
dgn-np:NP495118.RAN3yrA7oSyE6EG1mvCcfPrbFBLeJrXCBaYDes397ZkRA130_assertion
;
np:hasProvenance
dgn-np:NP495118.RAN3yrA7oSyE6EG1mvCcfPrbFBLeJrXCBaYDes397ZkRA130_provenance
;
np:hasPublicationInfo
dgn-np:NP495118.RAN3yrA7oSyE6EG1mvCcfPrbFBLeJrXCBaYDes397ZkRA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP495118.RAN3yrA7oSyE6EG1mvCcfPrbFBLeJrXCBaYDes397ZkRA130_assertion
a
np:Assertion
.
dgn-np:NP495118.RAN3yrA7oSyE6EG1mvCcfPrbFBLeJrXCBaYDes397ZkRA130_provenance
a
np:Provenance
.
dgn-np:NP495118.RAN3yrA7oSyE6EG1mvCcfPrbFBLeJrXCBaYDes397ZkRA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP495118.RAN3yrA7oSyE6EG1mvCcfPrbFBLeJrXCBaYDes397ZkRA130_assertion
{
miriam-gene:23263
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN73af216b0d3b9a8ff4831fbbcd38f842
sio:SIO_000628
miriam-gene:23263
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP495118.RAN3yrA7oSyE6EG1mvCcfPrbFBLeJrXCBaYDes397ZkRA130_provenance
{
dgn-np:NP495118.RAN3yrA7oSyE6EG1mvCcfPrbFBLeJrXCBaYDes397ZkRA130_assertion
dcterms:description
"[Several of the most significantly altered loci (CAV1, EVX1, MCF2L, and FGF1) were then used as probes to map the extent of these DNA methylation changes in normal tissues from prostates containing cancer.]. 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:23555185
;
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:NP495118.RAN3yrA7oSyE6EG1mvCcfPrbFBLeJrXCBaYDes397ZkRA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:55+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" .
}