@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP45941.RApO1TZT_1fXq5vZntkF43cGcGvbOax6r09P1tfjUXcHM
> .
@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 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:NP45941.RApO1TZT_1fXq5vZntkF43cGcGvbOax6r09P1tfjUXcHM130_head
{
this:
np:hasAssertion
dgn-np:NP45941.RApO1TZT_1fXq5vZntkF43cGcGvbOax6r09P1tfjUXcHM130_assertion
;
np:hasProvenance
dgn-np:NP45941.RApO1TZT_1fXq5vZntkF43cGcGvbOax6r09P1tfjUXcHM130_provenance
;
np:hasPublicationInfo
dgn-np:NP45941.RApO1TZT_1fXq5vZntkF43cGcGvbOax6r09P1tfjUXcHM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP45941.RApO1TZT_1fXq5vZntkF43cGcGvbOax6r09P1tfjUXcHM130_assertion
a
np:Assertion
.
dgn-np:NP45941.RApO1TZT_1fXq5vZntkF43cGcGvbOax6r09P1tfjUXcHM130_provenance
a
np:Provenance
.
dgn-np:NP45941.RApO1TZT_1fXq5vZntkF43cGcGvbOax6r09P1tfjUXcHM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP45941.RApO1TZT_1fXq5vZntkF43cGcGvbOax6r09P1tfjUXcHM130_assertion
{
miriam-gene:1545
a
ncit:C16612
.
lld:C0017601
a
ncit:C7057
.
dgn-gda:DGNfc5952c354a202104c0875c044b63df2
sio:SIO_000628
miriam-gene:1545
,
lld:C0017601
;
a
sio:SIO_001122
.
}
dgn-np:NP45941.RApO1TZT_1fXq5vZntkF43cGcGvbOax6r09P1tfjUXcHM130_provenance
{
dgn-np:NP45941.RApO1TZT_1fXq5vZntkF43cGcGvbOax6r09P1tfjUXcHM130_assertion
dct:description
"[Our results indicate that only a minor proportion of German PCG patients harbor mutations in the CYP1B1 gene and are in line with similar studies from other ethnic populations in which the rate of consanguinity is low.]. 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:19195637
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP45941.RApO1TZT_1fXq5vZntkF43cGcGvbOax6r09P1tfjUXcHM130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:21+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}