@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP322989.RAJ7Vx_b0zQVWjmKawMUdpDhyRCB44nvN3F7HeGKL7bQE
> .
@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:NP322989.RAJ7Vx_b0zQVWjmKawMUdpDhyRCB44nvN3F7HeGKL7bQE130_head
{
this:
np:hasAssertion
dgn-np:NP322989.RAJ7Vx_b0zQVWjmKawMUdpDhyRCB44nvN3F7HeGKL7bQE130_assertion
;
np:hasProvenance
dgn-np:NP322989.RAJ7Vx_b0zQVWjmKawMUdpDhyRCB44nvN3F7HeGKL7bQE130_provenance
;
np:hasPublicationInfo
dgn-np:NP322989.RAJ7Vx_b0zQVWjmKawMUdpDhyRCB44nvN3F7HeGKL7bQE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP322989.RAJ7Vx_b0zQVWjmKawMUdpDhyRCB44nvN3F7HeGKL7bQE130_assertion
a
np:Assertion
.
dgn-np:NP322989.RAJ7Vx_b0zQVWjmKawMUdpDhyRCB44nvN3F7HeGKL7bQE130_provenance
a
np:Provenance
.
dgn-np:NP322989.RAJ7Vx_b0zQVWjmKawMUdpDhyRCB44nvN3F7HeGKL7bQE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP322989.RAJ7Vx_b0zQVWjmKawMUdpDhyRCB44nvN3F7HeGKL7bQE130_assertion
{
miriam-gene:4397
a
ncit:C16612
.
lld:C0085584
a
ncit:C7057
.
dgn-gda:DGNf708831262c1a91503747c1a73e83eec
sio:SIO_000628
miriam-gene:4397
,
lld:C0085584
;
a
sio:SIO_001121
.
}
dgn-np:NP322989.RAJ7Vx_b0zQVWjmKawMUdpDhyRCB44nvN3F7HeGKL7bQE130_provenance
{
dgn-np:NP322989.RAJ7Vx_b0zQVWjmKawMUdpDhyRCB44nvN3F7HeGKL7bQE130_assertion
dcterms:description
"[Evidence is now available to support this scenario for neurological disorders such as Alzheimer's disease, amyotrophic lateral sclerosis, Parkinson's disease, multiple sclerosis and Huntington's disease, but also in the brain damage following ischemia and reperfusion, Down's syndrome and mitochondrial encephalopathies.]. 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:15341181
;
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:NP322989.RAJ7Vx_b0zQVWjmKawMUdpDhyRCB44nvN3F7HeGKL7bQE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:09+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" .
}