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http://rdf.disgenet.org/nanopublications.trig#NP456410.RAChJwtHoG2UOjEx0YMzgjNXqHjWsMgsSbirM8zu1eBek
> .
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http://www.w3.org/2000/01/rdf-schema#
> .
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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#
> .
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http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
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{
this:
np:hasAssertion
dgn-np:NP456410.RAChJwtHoG2UOjEx0YMzgjNXqHjWsMgsSbirM8zu1eBek130_assertion
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dgn-np:NP456410.RAChJwtHoG2UOjEx0YMzgjNXqHjWsMgsSbirM8zu1eBek130_publicationInfo
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a
np:Nanopublication
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a
np:Assertion
.
dgn-np:NP456410.RAChJwtHoG2UOjEx0YMzgjNXqHjWsMgsSbirM8zu1eBek130_provenance
a
np:Provenance
.
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np:PublicationInfo
.
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{
miriam-gene:1589
a
ncit:C16612
.
lld:C0206081
a
ncit:C7057
.
dgn-gda:DGNdd7a1335532f0417aa555e5fb130ebaa
sio:SIO_000628
miriam-gene:1589
,
lld:C0206081
;
a
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.
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dgn-np:NP456410.RAChJwtHoG2UOjEx0YMzgjNXqHjWsMgsSbirM8zu1eBek130_provenance
{
dgn-np:NP456410.RAChJwtHoG2UOjEx0YMzgjNXqHjWsMgsSbirM8zu1eBek130_assertion
dcterms:description
"[To begin the search for modifying loci responsible for this phenotypic heterogeneity, we performed CYP21 genotype analysis and assays for three candidate modifier loci on genomic DNA samples obtained from 30 adolescent girls with hyperandrogenism, 14 healthy control women, and 15 female obligate CYP21 mutation carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:11117678
;
prov:wasDerivedFrom
dgn-void:befree-20140225
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prov:wasGeneratedBy
eco:ECO_0000203
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dgn-void:befree-20140225
pav:importedOn
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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
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dgn-np:NP456410.RAChJwtHoG2UOjEx0YMzgjNXqHjWsMgsSbirM8zu1eBek130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
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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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> , <
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> , <
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> , <
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> ;
pav:createdBy
<
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