@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP669243.RA7iYV0UYPqqok0nZwV1lNLApWImypwcqb9Yn-F700M38
> .
@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:NP669243.RA7iYV0UYPqqok0nZwV1lNLApWImypwcqb9Yn-F700M38130_head
{
this:
np:hasAssertion
dgn-np:NP669243.RA7iYV0UYPqqok0nZwV1lNLApWImypwcqb9Yn-F700M38130_assertion
;
np:hasProvenance
dgn-np:NP669243.RA7iYV0UYPqqok0nZwV1lNLApWImypwcqb9Yn-F700M38130_provenance
;
np:hasPublicationInfo
dgn-np:NP669243.RA7iYV0UYPqqok0nZwV1lNLApWImypwcqb9Yn-F700M38130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP669243.RA7iYV0UYPqqok0nZwV1lNLApWImypwcqb9Yn-F700M38130_assertion
a
np:Assertion
.
dgn-np:NP669243.RA7iYV0UYPqqok0nZwV1lNLApWImypwcqb9Yn-F700M38130_provenance
a
np:Provenance
.
dgn-np:NP669243.RA7iYV0UYPqqok0nZwV1lNLApWImypwcqb9Yn-F700M38130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP669243.RA7iYV0UYPqqok0nZwV1lNLApWImypwcqb9Yn-F700M38130_assertion
{
miriam-gene:869
a
ncit:C16612
.
lld:C1527231
a
ncit:C7057
.
dgn-gda:DGN1dabcebafb980a2412bc42a26bae17ee
sio:SIO_000628
miriam-gene:869
,
lld:C1527231
;
a
sio:SIO_001121
.
}
dgn-np:NP669243.RA7iYV0UYPqqok0nZwV1lNLApWImypwcqb9Yn-F700M38130_provenance
{
dgn-np:NP669243.RA7iYV0UYPqqok0nZwV1lNLApWImypwcqb9Yn-F700M38130_assertion
dcterms:description
"[The two most common forms of X-ALD are the cerebral (CER) form, with an inflammatory demyelinating reaction that resembles multiple sclerosis (MS), and adrenomyeloneuropathy (AMN), which involves the spinal cord and in which the inflammatory reaction is mild or absent.]. 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:10604233
;
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:NP669243.RA7iYV0UYPqqok0nZwV1lNLApWImypwcqb9Yn-F700M38130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:44+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" .
}