@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP48705.RAd4uL0vF4boK2mqmCn117wRUFSs8ApG8vTkIREbGPb8E
> .
@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:NP48705.RAd4uL0vF4boK2mqmCn117wRUFSs8ApG8vTkIREbGPb8E130_head
{
this:
np:hasAssertion
dgn-np:NP48705.RAd4uL0vF4boK2mqmCn117wRUFSs8ApG8vTkIREbGPb8E130_assertion
;
np:hasProvenance
dgn-np:NP48705.RAd4uL0vF4boK2mqmCn117wRUFSs8ApG8vTkIREbGPb8E130_provenance
;
np:hasPublicationInfo
dgn-np:NP48705.RAd4uL0vF4boK2mqmCn117wRUFSs8ApG8vTkIREbGPb8E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP48705.RAd4uL0vF4boK2mqmCn117wRUFSs8ApG8vTkIREbGPb8E130_assertion
a
np:Assertion
.
dgn-np:NP48705.RAd4uL0vF4boK2mqmCn117wRUFSs8ApG8vTkIREbGPb8E130_provenance
a
np:Provenance
.
dgn-np:NP48705.RAd4uL0vF4boK2mqmCn117wRUFSs8ApG8vTkIREbGPb8E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP48705.RAd4uL0vF4boK2mqmCn117wRUFSs8ApG8vTkIREbGPb8E130_assertion
{
miriam-gene:210
a
ncit:C16612
.
lld:C0153633
a
ncit:C7057
.
dgn-gda:DGNf8de4d6bd33f523caab40b5f3929f2ad
sio:SIO_000628
miriam-gene:210
,
lld:C0153633
;
a
sio:SIO_001122
.
}
dgn-np:NP48705.RAd4uL0vF4boK2mqmCn117wRUFSs8ApG8vTkIREbGPb8E130_provenance
{
dgn-np:NP48705.RAd4uL0vF4boK2mqmCn117wRUFSs8ApG8vTkIREbGPb8E130_assertion
dcterms:description
"[Although our results indicate that lead may be implicated in meningioma risk in genetically susceptible individuals, these results need to be interpreted with caution given the small numbers of exposed cases with a variant genotype.]. 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:17164378
;
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:NP48705.RAd4uL0vF4boK2mqmCn117wRUFSs8ApG8vTkIREbGPb8E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:22+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" .
}