@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP423201.RAX53aB8J7gCdNXlAF4WP9soXiuImZu1-wY6Iee0Uy5Ko
> .
@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:NP423201.RAX53aB8J7gCdNXlAF4WP9soXiuImZu1-wY6Iee0Uy5Ko130_head
{
this:
np:hasAssertion
dgn-np:NP423201.RAX53aB8J7gCdNXlAF4WP9soXiuImZu1-wY6Iee0Uy5Ko130_assertion
;
np:hasProvenance
dgn-np:NP423201.RAX53aB8J7gCdNXlAF4WP9soXiuImZu1-wY6Iee0Uy5Ko130_provenance
;
np:hasPublicationInfo
dgn-np:NP423201.RAX53aB8J7gCdNXlAF4WP9soXiuImZu1-wY6Iee0Uy5Ko130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP423201.RAX53aB8J7gCdNXlAF4WP9soXiuImZu1-wY6Iee0Uy5Ko130_assertion
a
np:Assertion
.
dgn-np:NP423201.RAX53aB8J7gCdNXlAF4WP9soXiuImZu1-wY6Iee0Uy5Ko130_provenance
a
np:Provenance
.
dgn-np:NP423201.RAX53aB8J7gCdNXlAF4WP9soXiuImZu1-wY6Iee0Uy5Ko130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP423201.RAX53aB8J7gCdNXlAF4WP9soXiuImZu1-wY6Iee0Uy5Ko130_assertion
{
miriam-gene:2670
a
ncit:C16612
.
lld:C0524851
a
ncit:C7057
.
dgn-gda:DGN26b3850ab02f9746f8be382f3fb03c23
sio:SIO_000628
miriam-gene:2670
,
lld:C0524851
;
a
sio:SIO_001121
.
}
dgn-np:NP423201.RAX53aB8J7gCdNXlAF4WP9soXiuImZu1-wY6Iee0Uy5Ko130_provenance
{
dgn-np:NP423201.RAX53aB8J7gCdNXlAF4WP9soXiuImZu1-wY6Iee0Uy5Ko130_assertion
dcterms:description
"[Alexander disease (AxD) is a rare neurodegenerative disorder characterized pathologically by the presence of eosinophilic inclusions known as Rosenthal fibers (RFs) within astrocytes, and is caused by dominant mutations in the coding region of the gene encoding glial fibrillary acidic protein (GFAP).]. 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:24806671
;
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:NP423201.RAX53aB8J7gCdNXlAF4WP9soXiuImZu1-wY6Iee0Uy5Ko130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:41:46+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: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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}