@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP48055.RAmuzoTB32u3Phe6LirZBZVTy3NcMiRhR0HbxFRg0tENE
> .
@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 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:NP48055.RAmuzoTB32u3Phe6LirZBZVTy3NcMiRhR0HbxFRg0tENE130_head
{
this:
np:hasAssertion
dgn-np:NP48055.RAmuzoTB32u3Phe6LirZBZVTy3NcMiRhR0HbxFRg0tENE130_assertion
;
np:hasProvenance
dgn-np:NP48055.RAmuzoTB32u3Phe6LirZBZVTy3NcMiRhR0HbxFRg0tENE130_provenance
;
np:hasPublicationInfo
dgn-np:NP48055.RAmuzoTB32u3Phe6LirZBZVTy3NcMiRhR0HbxFRg0tENE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP48055.RAmuzoTB32u3Phe6LirZBZVTy3NcMiRhR0HbxFRg0tENE130_assertion
a
np:Assertion
.
dgn-np:NP48055.RAmuzoTB32u3Phe6LirZBZVTy3NcMiRhR0HbxFRg0tENE130_provenance
a
np:Provenance
.
dgn-np:NP48055.RAmuzoTB32u3Phe6LirZBZVTy3NcMiRhR0HbxFRg0tENE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP48055.RAmuzoTB32u3Phe6LirZBZVTy3NcMiRhR0HbxFRg0tENE130_assertion
{
miriam-gene:367
a
ncit:C16612
.
lld:C0162311
a
ncit:C7057
.
dgn-gda:DGN59609fed5f1cb47fb6a92e13308125fe
sio:SIO_000628
miriam-gene:367
,
lld:C0162311
;
a
sio:SIO_001122
.
}
dgn-np:NP48055.RAmuzoTB32u3Phe6LirZBZVTy3NcMiRhR0HbxFRg0tENE130_provenance
{
dgn-np:NP48055.RAmuzoTB32u3Phe6LirZBZVTy3NcMiRhR0HbxFRg0tENE130_assertion
dct:description
"[To determine if the androgen receptor gene is associated with male pattern baldness, we compared allele frequencies of the androgen receptor gene polymorphisms (StuI restriction fragment length polymorphism and two triplet repeat polymorphisms) in cases with cosmetically significant baldness (54 young and 392 older men) and controls (107 older men) with no indication of baldness.]. 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:11231320
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP48055.RAmuzoTB32u3Phe6LirZBZVTy3NcMiRhR0HbxFRg0tENE130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:22+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}