@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP352958.RApVrdATqccCVXAZhlfTdbHaVTNi3wvWoZxDGrsrcW5mY
> .
@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:NP352958.RApVrdATqccCVXAZhlfTdbHaVTNi3wvWoZxDGrsrcW5mY130_head
{
this:
np:hasAssertion
dgn-np:NP352958.RApVrdATqccCVXAZhlfTdbHaVTNi3wvWoZxDGrsrcW5mY130_assertion
;
np:hasProvenance
dgn-np:NP352958.RApVrdATqccCVXAZhlfTdbHaVTNi3wvWoZxDGrsrcW5mY130_provenance
;
np:hasPublicationInfo
dgn-np:NP352958.RApVrdATqccCVXAZhlfTdbHaVTNi3wvWoZxDGrsrcW5mY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP352958.RApVrdATqccCVXAZhlfTdbHaVTNi3wvWoZxDGrsrcW5mY130_assertion
a
np:Assertion
.
dgn-np:NP352958.RApVrdATqccCVXAZhlfTdbHaVTNi3wvWoZxDGrsrcW5mY130_provenance
a
np:Provenance
.
dgn-np:NP352958.RApVrdATqccCVXAZhlfTdbHaVTNi3wvWoZxDGrsrcW5mY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP352958.RApVrdATqccCVXAZhlfTdbHaVTNi3wvWoZxDGrsrcW5mY130_assertion
{
miriam-gene:367
a
ncit:C16612
.
lld:C0042755
a
ncit:C7057
.
dgn-gda:DGN972992a8bea9127cbf05944e1f79d5f4
sio:SIO_000628
miriam-gene:367
,
lld:C0042755
;
a
sio:SIO_001121
.
}
dgn-np:NP352958.RApVrdATqccCVXAZhlfTdbHaVTNi3wvWoZxDGrsrcW5mY130_provenance
{
dgn-np:NP352958.RApVrdATqccCVXAZhlfTdbHaVTNi3wvWoZxDGrsrcW5mY130_assertion
dcterms:description
"[In addition, there was no difference in lengths of the polymorphic CAG repeat in the AR gene between CAH girls with the I172N mutation who showed minimal and severe virilization, and we found no evidence of skewed X-inactivation.]. 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:12050225
;
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:NP352958.RApVrdATqccCVXAZhlfTdbHaVTNi3wvWoZxDGrsrcW5mY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:27+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" .
}