@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP608857.RAHgwrWo2CaJyhjMBbd16ALjIZLb67KSemF-9_RbhWm5A
> .
@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:NP608857.RAHgwrWo2CaJyhjMBbd16ALjIZLb67KSemF-9_RbhWm5A130_head
{
this:
np:hasAssertion
dgn-np:NP608857.RAHgwrWo2CaJyhjMBbd16ALjIZLb67KSemF-9_RbhWm5A130_assertion
;
np:hasProvenance
dgn-np:NP608857.RAHgwrWo2CaJyhjMBbd16ALjIZLb67KSemF-9_RbhWm5A130_provenance
;
np:hasPublicationInfo
dgn-np:NP608857.RAHgwrWo2CaJyhjMBbd16ALjIZLb67KSemF-9_RbhWm5A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP608857.RAHgwrWo2CaJyhjMBbd16ALjIZLb67KSemF-9_RbhWm5A130_assertion
a
np:Assertion
.
dgn-np:NP608857.RAHgwrWo2CaJyhjMBbd16ALjIZLb67KSemF-9_RbhWm5A130_provenance
a
np:Provenance
.
dgn-np:NP608857.RAHgwrWo2CaJyhjMBbd16ALjIZLb67KSemF-9_RbhWm5A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP608857.RAHgwrWo2CaJyhjMBbd16ALjIZLb67KSemF-9_RbhWm5A130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGNfb3224ad816e29e57c757494f161d553
sio:SIO_000628
miriam-gene:3077
,
lld:C0030567
;
a
sio:SIO_001121
.
}
dgn-np:NP608857.RAHgwrWo2CaJyhjMBbd16ALjIZLb67KSemF-9_RbhWm5A130_provenance
{
dgn-np:NP608857.RAHgwrWo2CaJyhjMBbd16ALjIZLb67KSemF-9_RbhWm5A130_assertion
dcterms:description
"[We examined four known polymorphisms, C282Y and H63D in the HFE gene, G258S in the TF gene and S82G in the TFR gene, in 181 sporadic PD patients and 180 controls from Southern Italy to investigate their possible role in susceptibility to PD.]. 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:21384276
;
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:NP608857.RAHgwrWo2CaJyhjMBbd16ALjIZLb67KSemF-9_RbhWm5A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:05+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" .
}