@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP292557.RAKHr6Qfdw-wtPgi2UiSi8ibkaL_yv7IkkCe9bi31eUmo
> .
@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:NP292557.RAKHr6Qfdw-wtPgi2UiSi8ibkaL_yv7IkkCe9bi31eUmo130_head
{
this:
np:hasAssertion
dgn-np:NP292557.RAKHr6Qfdw-wtPgi2UiSi8ibkaL_yv7IkkCe9bi31eUmo130_assertion
;
np:hasProvenance
dgn-np:NP292557.RAKHr6Qfdw-wtPgi2UiSi8ibkaL_yv7IkkCe9bi31eUmo130_provenance
;
np:hasPublicationInfo
dgn-np:NP292557.RAKHr6Qfdw-wtPgi2UiSi8ibkaL_yv7IkkCe9bi31eUmo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP292557.RAKHr6Qfdw-wtPgi2UiSi8ibkaL_yv7IkkCe9bi31eUmo130_assertion
a
np:Assertion
.
dgn-np:NP292557.RAKHr6Qfdw-wtPgi2UiSi8ibkaL_yv7IkkCe9bi31eUmo130_provenance
a
np:Provenance
.
dgn-np:NP292557.RAKHr6Qfdw-wtPgi2UiSi8ibkaL_yv7IkkCe9bi31eUmo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP292557.RAKHr6Qfdw-wtPgi2UiSi8ibkaL_yv7IkkCe9bi31eUmo130_assertion
{
miriam-gene:1594
a
ncit:C16612
.
lld:C0026764
a
ncit:C7057
.
dgn-gda:DGNb6a047342f1e3986805a30784445515e
sio:SIO_000628
miriam-gene:1594
,
lld:C0026764
;
a
sio:SIO_001121
.
}
dgn-np:NP292557.RAKHr6Qfdw-wtPgi2UiSi8ibkaL_yv7IkkCe9bi31eUmo130_provenance
{
dgn-np:NP292557.RAKHr6Qfdw-wtPgi2UiSi8ibkaL_yv7IkkCe9bi31eUmo130_assertion
dcterms:description
"[The purpose of this study is to ascertain whether VDR genotype which is involved in the risk for many cancers including multiple myeloma is also correlated with cancers in patients with Gaucher disease.]. 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:20920864
;
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:NP292557.RAKHr6Qfdw-wtPgi2UiSi8ibkaL_yv7IkkCe9bi31eUmo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:46+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" .
}