@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP428311.RA8KYav32zNcbZ-3jQNceGR7iEhPeguqXPG4cpOy8grW4
> .
@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:NP428311.RA8KYav32zNcbZ-3jQNceGR7iEhPeguqXPG4cpOy8grW4130_head
{
this:
np:hasAssertion
dgn-np:NP428311.RA8KYav32zNcbZ-3jQNceGR7iEhPeguqXPG4cpOy8grW4130_assertion
;
np:hasProvenance
dgn-np:NP428311.RA8KYav32zNcbZ-3jQNceGR7iEhPeguqXPG4cpOy8grW4130_provenance
;
np:hasPublicationInfo
dgn-np:NP428311.RA8KYav32zNcbZ-3jQNceGR7iEhPeguqXPG4cpOy8grW4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP428311.RA8KYav32zNcbZ-3jQNceGR7iEhPeguqXPG4cpOy8grW4130_assertion
a
np:Assertion
.
dgn-np:NP428311.RA8KYav32zNcbZ-3jQNceGR7iEhPeguqXPG4cpOy8grW4130_provenance
a
np:Provenance
.
dgn-np:NP428311.RA8KYav32zNcbZ-3jQNceGR7iEhPeguqXPG4cpOy8grW4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP428311.RA8KYav32zNcbZ-3jQNceGR7iEhPeguqXPG4cpOy8grW4130_assertion
{
miriam-gene:5176
a
ncit:C16612
.
lld:C0002736
a
ncit:C7057
.
dgn-gda:DGN73ed649330f680221ce82642ddf227ea
sio:SIO_000628
miriam-gene:5176
,
lld:C0002736
;
a
sio:SIO_001121
.
}
dgn-np:NP428311.RA8KYav32zNcbZ-3jQNceGR7iEhPeguqXPG4cpOy8grW4130_provenance
{
dgn-np:NP428311.RA8KYav32zNcbZ-3jQNceGR7iEhPeguqXPG4cpOy8grW4130_assertion
dcterms:description
"[These observations raise the possibility that application of PEDF may be helpful in designing new therapeutic strategies for neurodegenerative diseases such as amyotrophic lateral sclerosis, Parkinson's disease, Huntington's disease, Alzheimer's disease and brain ischemia.]. 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:20236058
;
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:NP428311.RA8KYav32zNcbZ-3jQNceGR7iEhPeguqXPG4cpOy8grW4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:14+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" .
}