@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP191753.RArkWGMs_kldA206rNaTL_JRWvIxoq2fXNP4wyldBZhjY
> .
@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:NP191753.RArkWGMs_kldA206rNaTL_JRWvIxoq2fXNP4wyldBZhjY130_head
{
this:
np:hasAssertion
dgn-np:NP191753.RArkWGMs_kldA206rNaTL_JRWvIxoq2fXNP4wyldBZhjY130_assertion
;
np:hasProvenance
dgn-np:NP191753.RArkWGMs_kldA206rNaTL_JRWvIxoq2fXNP4wyldBZhjY130_provenance
;
np:hasPublicationInfo
dgn-np:NP191753.RArkWGMs_kldA206rNaTL_JRWvIxoq2fXNP4wyldBZhjY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP191753.RArkWGMs_kldA206rNaTL_JRWvIxoq2fXNP4wyldBZhjY130_assertion
a
np:Assertion
.
dgn-np:NP191753.RArkWGMs_kldA206rNaTL_JRWvIxoq2fXNP4wyldBZhjY130_provenance
a
np:Provenance
.
dgn-np:NP191753.RArkWGMs_kldA206rNaTL_JRWvIxoq2fXNP4wyldBZhjY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP191753.RArkWGMs_kldA206rNaTL_JRWvIxoq2fXNP4wyldBZhjY130_assertion
{
miriam-gene:25824
a
ncit:C16612
.
lld:C0026769
a
ncit:C7057
.
dgn-gda:DGN38e15a436f429fb19ec0db8d53ac2e45
sio:SIO_000628
miriam-gene:25824
,
lld:C0026769
;
a
sio:SIO_001121
.
}
dgn-np:NP191753.RArkWGMs_kldA206rNaTL_JRWvIxoq2fXNP4wyldBZhjY130_provenance
{
dgn-np:NP191753.RArkWGMs_kldA206rNaTL_JRWvIxoq2fXNP4wyldBZhjY130_assertion
dcterms:description
"[Here we test the hypothesis that mutations in the human MBP and PLP genes might be associated with MS by examining the entire expressed sequence of both genes by single strand conformation polymorphism (SSCP) analysis, using a panel of 71 MS patients and 71 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:9460711
;
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:NP191753.RArkWGMs_kldA206rNaTL_JRWvIxoq2fXNP4wyldBZhjY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:45+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" .
}