@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP648976.RAumWse_nfE9OXUOetspUrx-PA4JX4dp86XHC2wC7-9HU
> .
@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:NP648976.RAumWse_nfE9OXUOetspUrx-PA4JX4dp86XHC2wC7-9HU130_head
{
this:
np:hasAssertion
dgn-np:NP648976.RAumWse_nfE9OXUOetspUrx-PA4JX4dp86XHC2wC7-9HU130_assertion
;
np:hasProvenance
dgn-np:NP648976.RAumWse_nfE9OXUOetspUrx-PA4JX4dp86XHC2wC7-9HU130_provenance
;
np:hasPublicationInfo
dgn-np:NP648976.RAumWse_nfE9OXUOetspUrx-PA4JX4dp86XHC2wC7-9HU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP648976.RAumWse_nfE9OXUOetspUrx-PA4JX4dp86XHC2wC7-9HU130_assertion
a
np:Assertion
.
dgn-np:NP648976.RAumWse_nfE9OXUOetspUrx-PA4JX4dp86XHC2wC7-9HU130_provenance
a
np:Provenance
.
dgn-np:NP648976.RAumWse_nfE9OXUOetspUrx-PA4JX4dp86XHC2wC7-9HU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP648976.RAumWse_nfE9OXUOetspUrx-PA4JX4dp86XHC2wC7-9HU130_assertion
{
miriam-gene:4397
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGNea18cb5201c7cb56c76a9a288f9a3fe4
sio:SIO_000628
miriam-gene:4397
,
lld:C0030567
;
a
sio:SIO_001121
.
}
dgn-np:NP648976.RAumWse_nfE9OXUOetspUrx-PA4JX4dp86XHC2wC7-9HU130_provenance
{
dgn-np:NP648976.RAumWse_nfE9OXUOetspUrx-PA4JX4dp86XHC2wC7-9HU130_assertion
dcterms:description
"[Further, this laboratory is utilizing the optimized sensitive procedure to search for several virus etiologies in human diseases such as multiple sclerosis, temporal lobe epilepsy, Alzheimer's disease, schizophrenia, and Parkinson's disease, as well as normal aging.]. 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:3299127
;
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:NP648976.RAumWse_nfE9OXUOetspUrx-PA4JX4dp86XHC2wC7-9HU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:31+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" .
}