@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP250093.RAF7nmwIGog7X818cj6vM99tLuQFnyi1BKWq--_u0LA7Y
> .
@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:NP250093.RAF7nmwIGog7X818cj6vM99tLuQFnyi1BKWq--_u0LA7Y130_head
{
this:
np:hasAssertion
dgn-np:NP250093.RAF7nmwIGog7X818cj6vM99tLuQFnyi1BKWq--_u0LA7Y130_assertion
;
np:hasProvenance
dgn-np:NP250093.RAF7nmwIGog7X818cj6vM99tLuQFnyi1BKWq--_u0LA7Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP250093.RAF7nmwIGog7X818cj6vM99tLuQFnyi1BKWq--_u0LA7Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP250093.RAF7nmwIGog7X818cj6vM99tLuQFnyi1BKWq--_u0LA7Y130_assertion
a
np:Assertion
.
dgn-np:NP250093.RAF7nmwIGog7X818cj6vM99tLuQFnyi1BKWq--_u0LA7Y130_provenance
a
np:Provenance
.
dgn-np:NP250093.RAF7nmwIGog7X818cj6vM99tLuQFnyi1BKWq--_u0LA7Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP250093.RAF7nmwIGog7X818cj6vM99tLuQFnyi1BKWq--_u0LA7Y130_assertion
{
miriam-gene:367
a
ncit:C16612
.
lld:C0020619
a
ncit:C7057
.
dgn-gda:DGN60f58e9cdee394fdbf89be74cc3ab593
sio:SIO_000628
miriam-gene:367
,
lld:C0020619
;
a
sio:SIO_001121
.
}
dgn-np:NP250093.RAF7nmwIGog7X818cj6vM99tLuQFnyi1BKWq--_u0LA7Y130_provenance
{
dgn-np:NP250093.RAF7nmwIGog7X818cj6vM99tLuQFnyi1BKWq--_u0LA7Y130_assertion
dcterms:description
"[Clinically, the (CAG)n polymorphism causes marked modulations of androgenicity in eugonadal men in various tissues and psychological traits and may cause the clinical picture of hypogonadism in the presence of normal testosterone concentrations.]. 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:19011288
;
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:NP250093.RAF7nmwIGog7X818cj6vM99tLuQFnyi1BKWq--_u0LA7Y130_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" .
}