@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP437326.RAmbElpBzTZFnAiE5MPlylh8PV8Dz1YftQ4qvUaOKEGMs
> .
@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:NP437326.RAmbElpBzTZFnAiE5MPlylh8PV8Dz1YftQ4qvUaOKEGMs130_head
{
this:
np:hasAssertion
dgn-np:NP437326.RAmbElpBzTZFnAiE5MPlylh8PV8Dz1YftQ4qvUaOKEGMs130_assertion
;
np:hasProvenance
dgn-np:NP437326.RAmbElpBzTZFnAiE5MPlylh8PV8Dz1YftQ4qvUaOKEGMs130_provenance
;
np:hasPublicationInfo
dgn-np:NP437326.RAmbElpBzTZFnAiE5MPlylh8PV8Dz1YftQ4qvUaOKEGMs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP437326.RAmbElpBzTZFnAiE5MPlylh8PV8Dz1YftQ4qvUaOKEGMs130_assertion
a
np:Assertion
.
dgn-np:NP437326.RAmbElpBzTZFnAiE5MPlylh8PV8Dz1YftQ4qvUaOKEGMs130_provenance
a
np:Provenance
.
dgn-np:NP437326.RAmbElpBzTZFnAiE5MPlylh8PV8Dz1YftQ4qvUaOKEGMs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP437326.RAmbElpBzTZFnAiE5MPlylh8PV8Dz1YftQ4qvUaOKEGMs130_assertion
{
miriam-gene:367
a
ncit:C16612
.
lld:C0042133
a
ncit:C7057
.
dgn-gda:DGNda6c5eb37c5d381cba3164c01732807c
sio:SIO_000628
miriam-gene:367
,
lld:C0042133
;
a
sio:SIO_001121
.
}
dgn-np:NP437326.RAmbElpBzTZFnAiE5MPlylh8PV8Dz1YftQ4qvUaOKEGMs130_provenance
{
dgn-np:NP437326.RAmbElpBzTZFnAiE5MPlylh8PV8Dz1YftQ4qvUaOKEGMs130_assertion
dcterms:description
"[Homozygous CAG repeats (22.0 +/- 2.3) in AR alleles were found in 5 of 30 cases, and either a large or small size of AR mRNA expression, were found in individual nodes of uterine leiomyoma, although paternal and maternal AR mRNAs from normal uterine myometrium were consistently expressed as AR alleles.]. 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:10601839
;
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:NP437326.RAmbElpBzTZFnAiE5MPlylh8PV8Dz1YftQ4qvUaOKEGMs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:19+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" .
}