@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP412772.RAzs98vSmp_lddcxmgLCkJN1G0HceT0vnKbcb0WaDvaa8
> .
@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:NP412772.RAzs98vSmp_lddcxmgLCkJN1G0HceT0vnKbcb0WaDvaa8130_head
{
this:
np:hasAssertion
dgn-np:NP412772.RAzs98vSmp_lddcxmgLCkJN1G0HceT0vnKbcb0WaDvaa8130_assertion
;
np:hasProvenance
dgn-np:NP412772.RAzs98vSmp_lddcxmgLCkJN1G0HceT0vnKbcb0WaDvaa8130_provenance
;
np:hasPublicationInfo
dgn-np:NP412772.RAzs98vSmp_lddcxmgLCkJN1G0HceT0vnKbcb0WaDvaa8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP412772.RAzs98vSmp_lddcxmgLCkJN1G0HceT0vnKbcb0WaDvaa8130_assertion
a
np:Assertion
.
dgn-np:NP412772.RAzs98vSmp_lddcxmgLCkJN1G0HceT0vnKbcb0WaDvaa8130_provenance
a
np:Provenance
.
dgn-np:NP412772.RAzs98vSmp_lddcxmgLCkJN1G0HceT0vnKbcb0WaDvaa8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP412772.RAzs98vSmp_lddcxmgLCkJN1G0HceT0vnKbcb0WaDvaa8130_assertion
{
miriam-gene:215
a
ncit:C16612
.
lld:C0011303
a
ncit:C7057
.
dgn-gda:DGN3e72a03a8c30cea5c876d1e5fc3169c6
sio:SIO_000628
miriam-gene:215
,
lld:C0011303
;
a
sio:SIO_001121
.
}
dgn-np:NP412772.RAzs98vSmp_lddcxmgLCkJN1G0HceT0vnKbcb0WaDvaa8130_provenance
{
dgn-np:NP412772.RAzs98vSmp_lddcxmgLCkJN1G0HceT0vnKbcb0WaDvaa8130_assertion
dcterms:description
"[X-linked adrenoleukodystrophy (ALD), an inherited demyelinating disorder of the central nervous system, can be corrected by allogeneic bone marrow transplantation, likely due to the turnover of brain macrophages that are bone marrow derived.]. 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:12668127
;
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:NP412772.RAzs98vSmp_lddcxmgLCkJN1G0HceT0vnKbcb0WaDvaa8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:05+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" .
}