@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP46152.RATho1d1MF5cRWLxRdyhblcfPmwFI8vsYMQ1zYRmJyXa0
> .
@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:NP46152.RATho1d1MF5cRWLxRdyhblcfPmwFI8vsYMQ1zYRmJyXa0130_head
{
this:
np:hasAssertion
dgn-np:NP46152.RATho1d1MF5cRWLxRdyhblcfPmwFI8vsYMQ1zYRmJyXa0130_assertion
;
np:hasProvenance
dgn-np:NP46152.RATho1d1MF5cRWLxRdyhblcfPmwFI8vsYMQ1zYRmJyXa0130_provenance
;
np:hasPublicationInfo
dgn-np:NP46152.RATho1d1MF5cRWLxRdyhblcfPmwFI8vsYMQ1zYRmJyXa0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP46152.RATho1d1MF5cRWLxRdyhblcfPmwFI8vsYMQ1zYRmJyXa0130_assertion
a
np:Assertion
.
dgn-np:NP46152.RATho1d1MF5cRWLxRdyhblcfPmwFI8vsYMQ1zYRmJyXa0130_provenance
a
np:Provenance
.
dgn-np:NP46152.RATho1d1MF5cRWLxRdyhblcfPmwFI8vsYMQ1zYRmJyXa0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP46152.RATho1d1MF5cRWLxRdyhblcfPmwFI8vsYMQ1zYRmJyXa0130_assertion
{
miriam-gene:1588
a
ncit:C16612
.
lld:C0014175
a
ncit:C7057
.
dgn-gda:DGN8a65c48c319c0e36b76846bae2f1573e
sio:SIO_000628
miriam-gene:1588
,
lld:C0014175
;
a
sio:SIO_001122
.
}
dgn-np:NP46152.RATho1d1MF5cRWLxRdyhblcfPmwFI8vsYMQ1zYRmJyXa0130_provenance
{
dgn-np:NP46152.RATho1d1MF5cRWLxRdyhblcfPmwFI8vsYMQ1zYRmJyXa0130_assertion
dcterms:description
"[ Our data suggest that CYP19 VNTR (TTTA)(10) allele as well as the combined genotype CYP1A1 m1 polymorphism and GSTM1 null deletion associate with the endometriosis phenotype, whereas the GSTT1 null deletion does not.]. 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:12620480
;
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:NP46152.RATho1d1MF5cRWLxRdyhblcfPmwFI8vsYMQ1zYRmJyXa0130_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" .
}