@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP783737.RAL9WtJ-CUM7CnbaVme8jyqdkduTl5_xm9ZIbxsDfoqws
> .
@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:NP783737.RAL9WtJ-CUM7CnbaVme8jyqdkduTl5_xm9ZIbxsDfoqws130_head
{
this:
np:hasAssertion
dgn-np:NP783737.RAL9WtJ-CUM7CnbaVme8jyqdkduTl5_xm9ZIbxsDfoqws130_assertion
;
np:hasProvenance
dgn-np:NP783737.RAL9WtJ-CUM7CnbaVme8jyqdkduTl5_xm9ZIbxsDfoqws130_provenance
;
np:hasPublicationInfo
dgn-np:NP783737.RAL9WtJ-CUM7CnbaVme8jyqdkduTl5_xm9ZIbxsDfoqws130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP783737.RAL9WtJ-CUM7CnbaVme8jyqdkduTl5_xm9ZIbxsDfoqws130_assertion
a
np:Assertion
.
dgn-np:NP783737.RAL9WtJ-CUM7CnbaVme8jyqdkduTl5_xm9ZIbxsDfoqws130_provenance
a
np:Provenance
.
dgn-np:NP783737.RAL9WtJ-CUM7CnbaVme8jyqdkduTl5_xm9ZIbxsDfoqws130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP783737.RAL9WtJ-CUM7CnbaVme8jyqdkduTl5_xm9ZIbxsDfoqws130_assertion
{
miriam-gene:869
a
ncit:C16612
.
lld:C0162309
a
ncit:C7057
.
dgn-gda:DGNa6212788b06d2531b9c4dc4325433aab
sio:SIO_000628
miriam-gene:869
,
lld:C0162309
;
a
sio:SIO_001121
.
}
dgn-np:NP783737.RAL9WtJ-CUM7CnbaVme8jyqdkduTl5_xm9ZIbxsDfoqws130_provenance
{
dgn-np:NP783737.RAL9WtJ-CUM7CnbaVme8jyqdkduTl5_xm9ZIbxsDfoqws130_assertion
dcterms:description
"[The two most common forms of X-linked adrenoleukodystrophy (X-ALD) are the cerebral forms (CER) with an inflammatory demyelinating reaction that resembles multiple sclerosis, and adrenomyeloneuropathy (AMN) which involves primarily 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:9143252
;
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:NP783737.RAL9WtJ-CUM7CnbaVme8jyqdkduTl5_xm9ZIbxsDfoqws130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:54+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" .
}