@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP167137.RAXxwjQjoDm94P9KIa6hEWCrUgkbUQwxALalBwrhe1S8Y
> .
@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:NP167137.RAXxwjQjoDm94P9KIa6hEWCrUgkbUQwxALalBwrhe1S8Y130_head
{
this:
np:hasAssertion
dgn-np:NP167137.RAXxwjQjoDm94P9KIa6hEWCrUgkbUQwxALalBwrhe1S8Y130_assertion
;
np:hasProvenance
dgn-np:NP167137.RAXxwjQjoDm94P9KIa6hEWCrUgkbUQwxALalBwrhe1S8Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP167137.RAXxwjQjoDm94P9KIa6hEWCrUgkbUQwxALalBwrhe1S8Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP167137.RAXxwjQjoDm94P9KIa6hEWCrUgkbUQwxALalBwrhe1S8Y130_assertion
a
np:Assertion
.
dgn-np:NP167137.RAXxwjQjoDm94P9KIa6hEWCrUgkbUQwxALalBwrhe1S8Y130_provenance
a
np:Provenance
.
dgn-np:NP167137.RAXxwjQjoDm94P9KIa6hEWCrUgkbUQwxALalBwrhe1S8Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP167137.RAXxwjQjoDm94P9KIa6hEWCrUgkbUQwxALalBwrhe1S8Y130_assertion
{
miriam-gene:1593
a
ncit:C16612
.
lld:C0004153
a
ncit:C7057
.
dgn-gda:DGN1ded2a331db667950e3235ae25278b6c
sio:SIO_000628
miriam-gene:1593
,
lld:C0004153
;
a
sio:SIO_001121
.
}
dgn-np:NP167137.RAXxwjQjoDm94P9KIa6hEWCrUgkbUQwxALalBwrhe1S8Y130_provenance
{
dgn-np:NP167137.RAXxwjQjoDm94P9KIa6hEWCrUgkbUQwxALalBwrhe1S8Y130_assertion
dcterms:description
"[A further impetus for exploring the normal biologic roles that are served by expression of the CYP27A1 gene is the knowledge that mutations in humans are associated with accelerated atherosclerosis and with severe neurologic impairment.]. 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:11111083
;
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:NP167137.RAXxwjQjoDm94P9KIa6hEWCrUgkbUQwxALalBwrhe1S8Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:30+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" .
}