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http://rdf.disgenet.org/nanopublications.trig#NP232390.RA_hRPP8xiQ8Ry_mPaXeN-CQ2Eq6A6Y5Lx80lPjB1FTCI
> .
@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:NP232390.RA_hRPP8xiQ8Ry_mPaXeN-CQ2Eq6A6Y5Lx80lPjB1FTCI130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP232390.RA_hRPP8xiQ8Ry_mPaXeN-CQ2Eq6A6Y5Lx80lPjB1FTCI130_publicationInfo
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a
np:Nanopublication
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a
np:Assertion
.
dgn-np:NP232390.RA_hRPP8xiQ8Ry_mPaXeN-CQ2Eq6A6Y5Lx80lPjB1FTCI130_provenance
a
np:Provenance
.
dgn-np:NP232390.RA_hRPP8xiQ8Ry_mPaXeN-CQ2Eq6A6Y5Lx80lPjB1FTCI130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:2670
a
ncit:C16612
.
lld:C0037772
a
ncit:C7057
.
dgn-gda:DGN9862e44a241c25c49c344fec7d8811bc
sio:SIO_000628
miriam-gene:2670
,
lld:C0037772
;
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.
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dgn-np:NP232390.RA_hRPP8xiQ8Ry_mPaXeN-CQ2Eq6A6Y5Lx80lPjB1FTCI130_provenance
{
dgn-np:NP232390.RA_hRPP8xiQ8Ry_mPaXeN-CQ2Eq6A6Y5Lx80lPjB1FTCI130_assertion
dcterms:description
"[This review centers on important recent advances in the understanding of the role of glial fibrillary acidic protein in Alexander disease and of proteolipid protein in hypomyelinating disorders such as Pelizaeus-Merzbacher and spastic paraplegia.]. 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:11723390
;
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 .
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dgn-np:NP232390.RA_hRPP8xiQ8Ry_mPaXeN-CQ2Eq6A6Y5Lx80lPjB1FTCI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:10+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
<
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> , <
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> , <
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> , <
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> ;
pav:createdBy
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"v2.1.0" .
}