@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP45904.RA0zTHTkOIdE00r86kSoW9pkzeDFwviu9_ECb6sjsHC2E
> .
@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:NP45904.RA0zTHTkOIdE00r86kSoW9pkzeDFwviu9_ECb6sjsHC2E130_head
{
this:
np:hasAssertion
dgn-np:NP45904.RA0zTHTkOIdE00r86kSoW9pkzeDFwviu9_ECb6sjsHC2E130_assertion
;
np:hasProvenance
dgn-np:NP45904.RA0zTHTkOIdE00r86kSoW9pkzeDFwviu9_ECb6sjsHC2E130_provenance
;
np:hasPublicationInfo
dgn-np:NP45904.RA0zTHTkOIdE00r86kSoW9pkzeDFwviu9_ECb6sjsHC2E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP45904.RA0zTHTkOIdE00r86kSoW9pkzeDFwviu9_ECb6sjsHC2E130_assertion
a
np:Assertion
.
dgn-np:NP45904.RA0zTHTkOIdE00r86kSoW9pkzeDFwviu9_ECb6sjsHC2E130_provenance
a
np:Provenance
.
dgn-np:NP45904.RA0zTHTkOIdE00r86kSoW9pkzeDFwviu9_ECb6sjsHC2E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP45904.RA0zTHTkOIdE00r86kSoW9pkzeDFwviu9_ECb6sjsHC2E130_assertion
{
miriam-gene:1545
a
ncit:C16612
.
lld:C0014130
a
ncit:C7057
.
dgn-gda:DGN305940df59a171fe78a8078263e5d9b1
sio:SIO_000628
miriam-gene:1545
,
lld:C0014130
;
a
sio:SIO_001122
.
}
dgn-np:NP45904.RA0zTHTkOIdE00r86kSoW9pkzeDFwviu9_ECb6sjsHC2E130_provenance
{
dgn-np:NP45904.RA0zTHTkOIdE00r86kSoW9pkzeDFwviu9_ECb6sjsHC2E130_assertion
dcterms:description
"[ Genetic variation in CYP19 and SHBG contributes to variance in circulating hormone levels between postmenopausal women, but low r2 values may explain why these genes have given inconclusive results in breast cancer case-control studies.]. 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:15199113
;
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:NP45904.RA0zTHTkOIdE00r86kSoW9pkzeDFwviu9_ECb6sjsHC2E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:21+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" .
}