@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP844490.RADK4H9xuBtj7EL9ErGjpggfS2Fo7O1C9G5htG1h9aBkg
> .
@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:NP844490.RADK4H9xuBtj7EL9ErGjpggfS2Fo7O1C9G5htG1h9aBkg130_head
{
this:
np:hasAssertion
dgn-np:NP844490.RADK4H9xuBtj7EL9ErGjpggfS2Fo7O1C9G5htG1h9aBkg130_assertion
;
np:hasProvenance
dgn-np:NP844490.RADK4H9xuBtj7EL9ErGjpggfS2Fo7O1C9G5htG1h9aBkg130_provenance
;
np:hasPublicationInfo
dgn-np:NP844490.RADK4H9xuBtj7EL9ErGjpggfS2Fo7O1C9G5htG1h9aBkg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP844490.RADK4H9xuBtj7EL9ErGjpggfS2Fo7O1C9G5htG1h9aBkg130_assertion
a
np:Assertion
.
dgn-np:NP844490.RADK4H9xuBtj7EL9ErGjpggfS2Fo7O1C9G5htG1h9aBkg130_provenance
a
np:Provenance
.
dgn-np:NP844490.RADK4H9xuBtj7EL9ErGjpggfS2Fo7O1C9G5htG1h9aBkg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP844490.RADK4H9xuBtj7EL9ErGjpggfS2Fo7O1C9G5htG1h9aBkg130_assertion
{
miriam-gene:1593
a
ncit:C16612
.
lld:C0025521
a
ncit:C7057
.
dgn-gda:DGNc7772181a8a0c6def352de3acd696f61
sio:SIO_000628
miriam-gene:1593
,
lld:C0025521
;
a
sio:SIO_001121
.
}
dgn-np:NP844490.RADK4H9xuBtj7EL9ErGjpggfS2Fo7O1C9G5htG1h9aBkg130_provenance
{
dgn-np:NP844490.RADK4H9xuBtj7EL9ErGjpggfS2Fo7O1C9G5htG1h9aBkg130_assertion
dcterms:description
"[Patients suffering from cerebrotendinous xanthomatosis (an autosomal recessive inborn error of metabolism) can easily be distinguished from patients not suffering from this disease, as the first excrete large amounts of the bile alcohol, 5 beta-cholestane-3 alpha,7 alpha,12 alpha,23,25-pentol, in urine, whereas the second do not.]. 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:3742821
;
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:NP844490.RADK4H9xuBtj7EL9ErGjpggfS2Fo7O1C9G5htG1h9aBkg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:36+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" .
}