@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP323835.RALoCeTXy0q16lLY-g83KmxCJoNspgXDlr1u3nKMVdaCI
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP323835.RALoCeTXy0q16lLY-g83KmxCJoNspgXDlr1u3nKMVdaCI130_assertion
;
np:hasProvenance
dgn-np:NP323835.RALoCeTXy0q16lLY-g83KmxCJoNspgXDlr1u3nKMVdaCI130_provenance
;
np:hasPublicationInfo
dgn-np:NP323835.RALoCeTXy0q16lLY-g83KmxCJoNspgXDlr1u3nKMVdaCI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP323835.RALoCeTXy0q16lLY-g83KmxCJoNspgXDlr1u3nKMVdaCI130_assertion
a
np:Assertion
.
dgn-np:NP323835.RALoCeTXy0q16lLY-g83KmxCJoNspgXDlr1u3nKMVdaCI130_provenance
a
np:Provenance
.
dgn-np:NP323835.RALoCeTXy0q16lLY-g83KmxCJoNspgXDlr1u3nKMVdaCI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP323835.RALoCeTXy0q16lLY-g83KmxCJoNspgXDlr1u3nKMVdaCI130_assertion
{
miriam-gene:57026
a
ncit:C16612
.
lld:C0026769
a
ncit:C7057
.
dgn-gda:DGN594e3139281d919280078e6b722baa79
sio:SIO_000628
miriam-gene:57026
,
lld:C0026769
;
a
sio:SIO_001121
.
}
dgn-np:NP323835.RALoCeTXy0q16lLY-g83KmxCJoNspgXDlr1u3nKMVdaCI130_provenance
{
dgn-np:NP323835.RALoCeTXy0q16lLY-g83KmxCJoNspgXDlr1u3nKMVdaCI130_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:NP323835.RALoCeTXy0q16lLY-g83KmxCJoNspgXDlr1u3nKMVdaCI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:09+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" .
}