@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP250526.RAsUev5lc2std0yrjPeXCb-gG9BsJ-OOD9p6kuc2CVx8w
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP250526.RAsUev5lc2std0yrjPeXCb-gG9BsJ-OOD9p6kuc2CVx8w130_head
{
this:
np:hasAssertion
dgn-np:NP250526.RAsUev5lc2std0yrjPeXCb-gG9BsJ-OOD9p6kuc2CVx8w130_assertion
;
np:hasProvenance
dgn-np:NP250526.RAsUev5lc2std0yrjPeXCb-gG9BsJ-OOD9p6kuc2CVx8w130_provenance
;
np:hasPublicationInfo
dgn-np:NP250526.RAsUev5lc2std0yrjPeXCb-gG9BsJ-OOD9p6kuc2CVx8w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP250526.RAsUev5lc2std0yrjPeXCb-gG9BsJ-OOD9p6kuc2CVx8w130_assertion
a
np:Assertion
.
dgn-np:NP250526.RAsUev5lc2std0yrjPeXCb-gG9BsJ-OOD9p6kuc2CVx8w130_provenance
a
np:Provenance
.
dgn-np:NP250526.RAsUev5lc2std0yrjPeXCb-gG9BsJ-OOD9p6kuc2CVx8w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP250526.RAsUev5lc2std0yrjPeXCb-gG9BsJ-OOD9p6kuc2CVx8w130_assertion
{
miriam-gene:367
a
ncit:C16612
.
lld:C0235832
a
ncit:C7057
.
dgn-gda:DGNae8797754c15c1d5505a4149d99f293f
sio:SIO_000628
miriam-gene:367
,
lld:C0235832
;
a
sio:SIO_001121
.
}
dgn-np:NP250526.RAsUev5lc2std0yrjPeXCb-gG9BsJ-OOD9p6kuc2CVx8w130_provenance
{
dgn-np:NP250526.RAsUev5lc2std0yrjPeXCb-gG9BsJ-OOD9p6kuc2CVx8w130_assertion
dcterms:description
"[Androgen receptor genotypes encoding moderate functional variation may influence cryptorchidism risk, particularly among boys with bilateral nondescent or congenital hernia, and may explain in part the elevated risk of testicular seminoma experienced by ex-cryptorchid boys.]. 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:22188741
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP250526.RAsUev5lc2std0yrjPeXCb-gG9BsJ-OOD9p6kuc2CVx8w130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:40:02+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}