@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP490923.RAuqfEVGFQHIkhSZI3lWPApjxydFbPbZqHxKEQ0WTfq_A
> .
@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:NP490923.RAuqfEVGFQHIkhSZI3lWPApjxydFbPbZqHxKEQ0WTfq_A130_head
{
this:
np:hasAssertion
dgn-np:NP490923.RAuqfEVGFQHIkhSZI3lWPApjxydFbPbZqHxKEQ0WTfq_A130_assertion
;
np:hasProvenance
dgn-np:NP490923.RAuqfEVGFQHIkhSZI3lWPApjxydFbPbZqHxKEQ0WTfq_A130_provenance
;
np:hasPublicationInfo
dgn-np:NP490923.RAuqfEVGFQHIkhSZI3lWPApjxydFbPbZqHxKEQ0WTfq_A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP490923.RAuqfEVGFQHIkhSZI3lWPApjxydFbPbZqHxKEQ0WTfq_A130_assertion
a
np:Assertion
.
dgn-np:NP490923.RAuqfEVGFQHIkhSZI3lWPApjxydFbPbZqHxKEQ0WTfq_A130_provenance
a
np:Provenance
.
dgn-np:NP490923.RAuqfEVGFQHIkhSZI3lWPApjxydFbPbZqHxKEQ0WTfq_A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP490923.RAuqfEVGFQHIkhSZI3lWPApjxydFbPbZqHxKEQ0WTfq_A130_assertion
{
miriam-gene:4155
a
ncit:C16612
.
lld:C0205711
a
ncit:C7057
.
dgn-gda:DGN6ca7b4c4f6b1f9b961bcedd97377ec90
sio:SIO_000628
miriam-gene:4155
,
lld:C0205711
;
a
sio:SIO_001121
.
}
dgn-np:NP490923.RAuqfEVGFQHIkhSZI3lWPApjxydFbPbZqHxKEQ0WTfq_A130_provenance
{
dgn-np:NP490923.RAuqfEVGFQHIkhSZI3lWPApjxydFbPbZqHxKEQ0WTfq_A130_assertion
dcterms:description
"[In a patient with connatal Pelizaeus-Merzbacher disease with the same mutation in the proteolipid protein gene as in jimpy(msd) mice the immunohistochemical study of the brain demonstrated deficiencies of myelin and proteolipid protein despite good expression of myelin basic protein.]. 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:10328282
;
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:NP490923.RAuqfEVGFQHIkhSZI3lWPApjxydFbPbZqHxKEQ0WTfq_A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:53+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" .
}