@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP42612.RALFa7jW9S7OmePgWBUVu-3P7toyaisYG3QXLJUG0-5dU
> .
@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:NP42612.RALFa7jW9S7OmePgWBUVu-3P7toyaisYG3QXLJUG0-5dU130_head
{
this:
np:hasAssertion
dgn-np:NP42612.RALFa7jW9S7OmePgWBUVu-3P7toyaisYG3QXLJUG0-5dU130_assertion
;
np:hasProvenance
dgn-np:NP42612.RALFa7jW9S7OmePgWBUVu-3P7toyaisYG3QXLJUG0-5dU130_provenance
;
np:hasPublicationInfo
dgn-np:NP42612.RALFa7jW9S7OmePgWBUVu-3P7toyaisYG3QXLJUG0-5dU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP42612.RALFa7jW9S7OmePgWBUVu-3P7toyaisYG3QXLJUG0-5dU130_assertion
a
np:Assertion
.
dgn-np:NP42612.RALFa7jW9S7OmePgWBUVu-3P7toyaisYG3QXLJUG0-5dU130_provenance
a
np:Provenance
.
dgn-np:NP42612.RALFa7jW9S7OmePgWBUVu-3P7toyaisYG3QXLJUG0-5dU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP42612.RALFa7jW9S7OmePgWBUVu-3P7toyaisYG3QXLJUG0-5dU130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGN6d2f50853e91b5595216a07bfebcf00e
sio:SIO_000628
miriam-gene:3077
,
lld:C0030567
;
a
sio:SIO_001122
.
}
dgn-np:NP42612.RALFa7jW9S7OmePgWBUVu-3P7toyaisYG3QXLJUG0-5dU130_provenance
{
dgn-np:NP42612.RALFa7jW9S7OmePgWBUVu-3P7toyaisYG3QXLJUG0-5dU130_assertion
dcterms:description
"[in the Italian population, the most common HFE mutations, H63D and C282Y are not associated with the individual risk to develop PD, nor have specific influence on the clinical features of the 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:18325820
;
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:NP42612.RALFa7jW9S7OmePgWBUVu-3P7toyaisYG3QXLJUG0-5dU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:19+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" .
}