@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP743132.RAM0cp0F4XXauAoRYjDQwSOKgcYq-fQWZnMxhg7CyJki8
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP743132.RAM0cp0F4XXauAoRYjDQwSOKgcYq-fQWZnMxhg7CyJki8130_head
{
this:
np:hasAssertion
dgn-np:NP743132.RAM0cp0F4XXauAoRYjDQwSOKgcYq-fQWZnMxhg7CyJki8130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP743132.RAM0cp0F4XXauAoRYjDQwSOKgcYq-fQWZnMxhg7CyJki8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP743132.RAM0cp0F4XXauAoRYjDQwSOKgcYq-fQWZnMxhg7CyJki8130_assertion
a
np:Assertion
.
dgn-np:NP743132.RAM0cp0F4XXauAoRYjDQwSOKgcYq-fQWZnMxhg7CyJki8130_provenance
a
np:Provenance
.
dgn-np:NP743132.RAM0cp0F4XXauAoRYjDQwSOKgcYq-fQWZnMxhg7CyJki8130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:7124
a
ncit:C16612
.
lld:C0002736
a
ncit:C7057
.
dgn-gda:DGN755a14e4ef634bad3c9f9b39147908cb
sio:SIO_000628
miriam-gene:7124
,
lld:C0002736
;
a
sio:SIO_001121
.
}
dgn-np:NP743132.RAM0cp0F4XXauAoRYjDQwSOKgcYq-fQWZnMxhg7CyJki8130_provenance
{
dgn-np:NP743132.RAM0cp0F4XXauAoRYjDQwSOKgcYq-fQWZnMxhg7CyJki8130_assertion
dcterms:description
"[This study was designed to detect wether the TNF2 allele is associated with disease progression in MS. We examined the TNFalpha -308 polymorphism with an allelic discrimination PCR to detect the G-->A transition in the genomic DNA of 283 MS patients from Germany and in 72 patients with amyotrophic lateral sclerosis (ALS) and 66 with stroke from the same genetic background who served as controls.]. 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:10552245
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP743132.RAM0cp0F4XXauAoRYjDQwSOKgcYq-fQWZnMxhg7CyJki8130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:45:08+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:disgenetv3.0rdf
;
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
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pav:version
"v3.0.0" .
}