@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP379675.RAYsIsXjHSp0Ex9FLigcOeaiWE7D5r10M2zb5WGerQrAw
> .
@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:NP379675.RAYsIsXjHSp0Ex9FLigcOeaiWE7D5r10M2zb5WGerQrAw130_head
{
this:
np:hasAssertion
dgn-np:NP379675.RAYsIsXjHSp0Ex9FLigcOeaiWE7D5r10M2zb5WGerQrAw130_assertion
;
np:hasProvenance
dgn-np:NP379675.RAYsIsXjHSp0Ex9FLigcOeaiWE7D5r10M2zb5WGerQrAw130_provenance
;
np:hasPublicationInfo
dgn-np:NP379675.RAYsIsXjHSp0Ex9FLigcOeaiWE7D5r10M2zb5WGerQrAw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP379675.RAYsIsXjHSp0Ex9FLigcOeaiWE7D5r10M2zb5WGerQrAw130_assertion
a
np:Assertion
.
dgn-np:NP379675.RAYsIsXjHSp0Ex9FLigcOeaiWE7D5r10M2zb5WGerQrAw130_provenance
a
np:Provenance
.
dgn-np:NP379675.RAYsIsXjHSp0Ex9FLigcOeaiWE7D5r10M2zb5WGerQrAw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP379675.RAYsIsXjHSp0Ex9FLigcOeaiWE7D5r10M2zb5WGerQrAw130_assertion
{
miriam-gene:64127
a
ncit:C16612
.
lld:C0026769
a
ncit:C7057
.
dgn-gda:DGN30b5707cc513d64756f39d74d6ef38ca
sio:SIO_000628
miriam-gene:64127
,
lld:C0026769
;
a
sio:SIO_001121
.
}
dgn-np:NP379675.RAYsIsXjHSp0Ex9FLigcOeaiWE7D5r10M2zb5WGerQrAw130_provenance
{
dgn-np:NP379675.RAYsIsXjHSp0Ex9FLigcOeaiWE7D5r10M2zb5WGerQrAw130_assertion
dcterms:description
"[As the CARD15 risk alleles had previously been assessed in our collection of 496 MS trios, we focused our efforts on the DLG5 risk allele and the IBD5(risk) haplotype (IBD5(risk)) for 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:16642031
;
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:NP379675.RAYsIsXjHSp0Ex9FLigcOeaiWE7D5r10M2zb5WGerQrAw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:44+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" .
}