@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP47857.RAyx8rhpQ0z2uC5OLso9zHSYbNPj8YVFCwLsqlNH0_2KA
> .
@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:NP47857.RAyx8rhpQ0z2uC5OLso9zHSYbNPj8YVFCwLsqlNH0_2KA130_head
{
this:
np:hasAssertion
dgn-np:NP47857.RAyx8rhpQ0z2uC5OLso9zHSYbNPj8YVFCwLsqlNH0_2KA130_assertion
;
np:hasProvenance
dgn-np:NP47857.RAyx8rhpQ0z2uC5OLso9zHSYbNPj8YVFCwLsqlNH0_2KA130_provenance
;
np:hasPublicationInfo
dgn-np:NP47857.RAyx8rhpQ0z2uC5OLso9zHSYbNPj8YVFCwLsqlNH0_2KA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP47857.RAyx8rhpQ0z2uC5OLso9zHSYbNPj8YVFCwLsqlNH0_2KA130_assertion
a
np:Assertion
.
dgn-np:NP47857.RAyx8rhpQ0z2uC5OLso9zHSYbNPj8YVFCwLsqlNH0_2KA130_provenance
a
np:Provenance
.
dgn-np:NP47857.RAyx8rhpQ0z2uC5OLso9zHSYbNPj8YVFCwLsqlNH0_2KA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP47857.RAyx8rhpQ0z2uC5OLso9zHSYbNPj8YVFCwLsqlNH0_2KA130_assertion
{
miriam-gene:598
a
ncit:C16612
.
lld:C0026769
a
ncit:C7057
.
dgn-gda:DGNa1c020e59634bc523b5e8c2be02a919e
sio:SIO_000628
miriam-gene:598
,
lld:C0026769
;
a
sio:SIO_001122
.
}
dgn-np:NP47857.RAyx8rhpQ0z2uC5OLso9zHSYbNPj8YVFCwLsqlNH0_2KA130_provenance
{
dgn-np:NP47857.RAyx8rhpQ0z2uC5OLso9zHSYbNPj8YVFCwLsqlNH0_2KA130_assertion
dcterms:description
"[No significant differences in the frequency of gene sequence variations were found between MS patients and controls. The apoptosis genes studied here therefore appear less likely to be important effector genes in MS.]. 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:12161031
;
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:NP47857.RAyx8rhpQ0z2uC5OLso9zHSYbNPj8YVFCwLsqlNH0_2KA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:22+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" .
}