@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP875287.RAdJSiEcwoau8bygYqkuR-RaTM6aaugl1dUv13Jkg7n7M
> .
@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:NP875287.RAdJSiEcwoau8bygYqkuR-RaTM6aaugl1dUv13Jkg7n7M130_head
{
this:
np:hasAssertion
dgn-np:NP875287.RAdJSiEcwoau8bygYqkuR-RaTM6aaugl1dUv13Jkg7n7M130_assertion
;
np:hasProvenance
dgn-np:NP875287.RAdJSiEcwoau8bygYqkuR-RaTM6aaugl1dUv13Jkg7n7M130_provenance
;
np:hasPublicationInfo
dgn-np:NP875287.RAdJSiEcwoau8bygYqkuR-RaTM6aaugl1dUv13Jkg7n7M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP875287.RAdJSiEcwoau8bygYqkuR-RaTM6aaugl1dUv13Jkg7n7M130_assertion
a
np:Assertion
.
dgn-np:NP875287.RAdJSiEcwoau8bygYqkuR-RaTM6aaugl1dUv13Jkg7n7M130_provenance
a
np:Provenance
.
dgn-np:NP875287.RAdJSiEcwoau8bygYqkuR-RaTM6aaugl1dUv13Jkg7n7M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP875287.RAdJSiEcwoau8bygYqkuR-RaTM6aaugl1dUv13Jkg7n7M130_assertion
{
miriam-gene:4609
a
ncit:C16612
.
lld:C2931456
a
ncit:C7057
.
dgn-gda:DGNb73e257152824f9981d4235cc472ac0a
sio:SIO_000628
miriam-gene:4609
,
lld:C2931456
;
a
sio:SIO_001121
.
}
dgn-np:NP875287.RAdJSiEcwoau8bygYqkuR-RaTM6aaugl1dUv13Jkg7n7M130_provenance
{
dgn-np:NP875287.RAdJSiEcwoau8bygYqkuR-RaTM6aaugl1dUv13Jkg7n7M130_assertion
dcterms:description
"[In families with multiple cases presenting with more aggressive disease, LOD scores over 3.0 were observed at 8q24 in the vicinity of previously identified common PC risk variants, as well as MYC, an important gene in PC biology.]. 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:21748754
;
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:NP875287.RAdJSiEcwoau8bygYqkuR-RaTM6aaugl1dUv13Jkg7n7M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:55+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" .
}