@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP71658.RAQH8T1TGiUYpYKve8516qAen7GyS76H6zC6F5xcKaXxc
> .
@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 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:NP71658.RAQH8T1TGiUYpYKve8516qAen7GyS76H6zC6F5xcKaXxc130_head
{
this:
np:hasAssertion
dgn-np:NP71658.RAQH8T1TGiUYpYKve8516qAen7GyS76H6zC6F5xcKaXxc130_assertion
;
np:hasProvenance
dgn-np:NP71658.RAQH8T1TGiUYpYKve8516qAen7GyS76H6zC6F5xcKaXxc130_provenance
;
np:hasPublicationInfo
dgn-np:NP71658.RAQH8T1TGiUYpYKve8516qAen7GyS76H6zC6F5xcKaXxc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP71658.RAQH8T1TGiUYpYKve8516qAen7GyS76H6zC6F5xcKaXxc130_assertion
a
np:Assertion
.
dgn-np:NP71658.RAQH8T1TGiUYpYKve8516qAen7GyS76H6zC6F5xcKaXxc130_provenance
a
np:Provenance
.
dgn-np:NP71658.RAQH8T1TGiUYpYKve8516qAen7GyS76H6zC6F5xcKaXxc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP71658.RAQH8T1TGiUYpYKve8516qAen7GyS76H6zC6F5xcKaXxc130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C0002736
a
ncit:C7057
.
dgn-gda:DGNe6dbec2af00629d6fcb0401ed6763b8a
sio:SIO_000628
miriam-gene:348
,
lld:C0002736
;
a
sio:SIO_001122
.
}
dgn-np:NP71658.RAQH8T1TGiUYpYKve8516qAen7GyS76H6zC6F5xcKaXxc130_provenance
{
dgn-np:NP71658.RAQH8T1TGiUYpYKve8516qAen7GyS76H6zC6F5xcKaXxc130_assertion
dct:description
"[It was shown that the frequency of the apoE-e2 allele was significantly higher in the young group characterized by more benign course of ALS (spinal variant, slow rate of progression of ALS and longer survival) as well as in patients with a more `benign` spinal form 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:19365373
;
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:NP71658.RAQH8T1TGiUYpYKve8516qAen7GyS76H6zC6F5xcKaXxc130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:34+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}