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http://rdf.disgenet.org/nanopublications.trig#NP817133.RADUHWZ44J613k-OBI2fQbWCjhYVbBC-8dLAGKttVsGEY
> .
@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
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;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP817133.RADUHWZ44J613k-OBI2fQbWCjhYVbBC-8dLAGKttVsGEY130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP817133.RADUHWZ44J613k-OBI2fQbWCjhYVbBC-8dLAGKttVsGEY130_assertion
a
np:Assertion
.
dgn-np:NP817133.RADUHWZ44J613k-OBI2fQbWCjhYVbBC-8dLAGKttVsGEY130_provenance
a
np:Provenance
.
dgn-np:NP817133.RADUHWZ44J613k-OBI2fQbWCjhYVbBC-8dLAGKttVsGEY130_publicationInfo
a
np:PublicationInfo
.
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dgn-np:NP817133.RADUHWZ44J613k-OBI2fQbWCjhYVbBC-8dLAGKttVsGEY130_assertion
{
miriam-gene:1437
a
ncit:C16612
.
lld:C0025517
a
ncit:C7057
.
dgn-gda:DGNf79ec9dedabc1853c40a6d0c956ac865
sio:SIO_000628
miriam-gene:1437
,
lld:C0025517
;
a
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.
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dgn-np:NP817133.RADUHWZ44J613k-OBI2fQbWCjhYVbBC-8dLAGKttVsGEY130_provenance
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dgn-np:NP817133.RADUHWZ44J613k-OBI2fQbWCjhYVbBC-8dLAGKttVsGEY130_assertion
dcterms:description
"[Although the results of molecular genetic and CSF studies are, at this time, unlikely to significantly alter clinical management of the patient, these analyses could be useful in providing information on prognosis (that is, DRD versus progressive neurodegenerative disorders or more severe metabolic disorders).]. 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:10495030
;
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:NP817133.RADUHWZ44J613k-OBI2fQbWCjhYVbBC-8dLAGKttVsGEY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:20+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
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pav:authoredBy
<
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> , <
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http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
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"v2.1.0" .
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