@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP861077.RAP6G6_la_u43j0-J8TPoNHVzKQDB2YLCbZhLqol7Ov2A
> .
@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:NP861077.RAP6G6_la_u43j0-J8TPoNHVzKQDB2YLCbZhLqol7Ov2A130_head
{
this:
np:hasAssertion
dgn-np:NP861077.RAP6G6_la_u43j0-J8TPoNHVzKQDB2YLCbZhLqol7Ov2A130_assertion
;
np:hasProvenance
dgn-np:NP861077.RAP6G6_la_u43j0-J8TPoNHVzKQDB2YLCbZhLqol7Ov2A130_provenance
;
np:hasPublicationInfo
dgn-np:NP861077.RAP6G6_la_u43j0-J8TPoNHVzKQDB2YLCbZhLqol7Ov2A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP861077.RAP6G6_la_u43j0-J8TPoNHVzKQDB2YLCbZhLqol7Ov2A130_assertion
a
np:Assertion
.
dgn-np:NP861077.RAP6G6_la_u43j0-J8TPoNHVzKQDB2YLCbZhLqol7Ov2A130_provenance
a
np:Provenance
.
dgn-np:NP861077.RAP6G6_la_u43j0-J8TPoNHVzKQDB2YLCbZhLqol7Ov2A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP861077.RAP6G6_la_u43j0-J8TPoNHVzKQDB2YLCbZhLqol7Ov2A130_assertion
{
miriam-gene:2078
a
ncit:C16612
.
lld:C0026769
a
ncit:C7057
.
dgn-gda:DGN1f9b95e5a29df8cb1e349ddff14f9811
sio:SIO_000628
miriam-gene:2078
,
lld:C0026769
;
a
sio:SIO_001121
.
}
dgn-np:NP861077.RAP6G6_la_u43j0-J8TPoNHVzKQDB2YLCbZhLqol7Ov2A130_provenance
{
dgn-np:NP861077.RAP6G6_la_u43j0-J8TPoNHVzKQDB2YLCbZhLqol7Ov2A130_assertion
dcterms:description
"[On the basis of these results, PvuII polymorphism might be associated with susceptibility to MS, and XbaI polymorphism with onset age of MS. ERG polymorphism should be further studied in other populations to improve strategies for treatment of 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:11054488
;
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:NP861077.RAP6G6_la_u43j0-J8TPoNHVzKQDB2YLCbZhLqol7Ov2A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:46+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" .
}