@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP303087.RAfzVHcWlgiiq8ud9MK1L2dY571WRwceDThWP77V-Vpp0
> .
@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:NP303087.RAfzVHcWlgiiq8ud9MK1L2dY571WRwceDThWP77V-Vpp0130_head
{
this:
np:hasAssertion
dgn-np:NP303087.RAfzVHcWlgiiq8ud9MK1L2dY571WRwceDThWP77V-Vpp0130_assertion
;
np:hasProvenance
dgn-np:NP303087.RAfzVHcWlgiiq8ud9MK1L2dY571WRwceDThWP77V-Vpp0130_provenance
;
np:hasPublicationInfo
dgn-np:NP303087.RAfzVHcWlgiiq8ud9MK1L2dY571WRwceDThWP77V-Vpp0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP303087.RAfzVHcWlgiiq8ud9MK1L2dY571WRwceDThWP77V-Vpp0130_assertion
a
np:Assertion
.
dgn-np:NP303087.RAfzVHcWlgiiq8ud9MK1L2dY571WRwceDThWP77V-Vpp0130_provenance
a
np:Provenance
.
dgn-np:NP303087.RAfzVHcWlgiiq8ud9MK1L2dY571WRwceDThWP77V-Vpp0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP303087.RAfzVHcWlgiiq8ud9MK1L2dY571WRwceDThWP77V-Vpp0130_assertion
{
miriam-gene:367
a
ncit:C16612
.
lld:C0238033
a
ncit:C7057
.
dgn-gda:DGN916f7468b101a96a3b0c067d5553bcef
sio:SIO_000628
miriam-gene:367
,
lld:C0238033
;
a
sio:SIO_001121
.
}
dgn-np:NP303087.RAfzVHcWlgiiq8ud9MK1L2dY571WRwceDThWP77V-Vpp0130_provenance
{
dgn-np:NP303087.RAfzVHcWlgiiq8ud9MK1L2dY571WRwceDThWP77V-Vpp0130_assertion
dcterms:description
"[In the present study, we have comprehensively screened the entire coding region of the AR gene for mutations and also studied the role of AR CAG and GGC repeat lengths as risk factors for MBC in a cohort of 32 Finnish MBC patients.]. 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:12602915
;
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:NP303087.RAfzVHcWlgiiq8ud9MK1L2dY571WRwceDThWP77V-Vpp0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:54+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" .
}