@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP790565.RANpWvrDLdI_8nBw8vxLY8NekHYFgMgtVGhakBSyoqR-M
> .
@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:NP790565.RANpWvrDLdI_8nBw8vxLY8NekHYFgMgtVGhakBSyoqR-M130_head
{
this:
np:hasAssertion
dgn-np:NP790565.RANpWvrDLdI_8nBw8vxLY8NekHYFgMgtVGhakBSyoqR-M130_assertion
;
np:hasProvenance
dgn-np:NP790565.RANpWvrDLdI_8nBw8vxLY8NekHYFgMgtVGhakBSyoqR-M130_provenance
;
np:hasPublicationInfo
dgn-np:NP790565.RANpWvrDLdI_8nBw8vxLY8NekHYFgMgtVGhakBSyoqR-M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP790565.RANpWvrDLdI_8nBw8vxLY8NekHYFgMgtVGhakBSyoqR-M130_assertion
a
np:Assertion
.
dgn-np:NP790565.RANpWvrDLdI_8nBw8vxLY8NekHYFgMgtVGhakBSyoqR-M130_provenance
a
np:Provenance
.
dgn-np:NP790565.RANpWvrDLdI_8nBw8vxLY8NekHYFgMgtVGhakBSyoqR-M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP790565.RANpWvrDLdI_8nBw8vxLY8NekHYFgMgtVGhakBSyoqR-M130_assertion
{
miriam-gene:6520
a
ncit:C16612
.
lld:C0027404
a
ncit:C7057
.
dgn-gda:DGNabe6655912b627f3f414c81b706827ad
sio:SIO_000628
miriam-gene:6520
,
lld:C0027404
;
a
sio:SIO_001121
.
}
dgn-np:NP790565.RANpWvrDLdI_8nBw8vxLY8NekHYFgMgtVGhakBSyoqR-M130_provenance
{
dgn-np:NP790565.RANpWvrDLdI_8nBw8vxLY8NekHYFgMgtVGhakBSyoqR-M130_assertion
dcterms:description
"[To determine if the IgH locus is involved in genetic predisposition to human narcolepsy, restriction fragment length polymorphisms specific for the IgM and IgG cluster within this locus were studied in sporadic cases of the disease, as well as in five families with two or more affected individuals.]. 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:8840222
;
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:NP790565.RANpWvrDLdI_8nBw8vxLY8NekHYFgMgtVGhakBSyoqR-M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:05+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" .
}