@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP601086.RALctX8cwb1Z_buvJK2JAoWqN7-3Ihg2l8bLsEL78xEmg
> .
@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:NP601086.RALctX8cwb1Z_buvJK2JAoWqN7-3Ihg2l8bLsEL78xEmg130_head
{
this:
np:hasAssertion
dgn-np:NP601086.RALctX8cwb1Z_buvJK2JAoWqN7-3Ihg2l8bLsEL78xEmg130_assertion
;
np:hasProvenance
dgn-np:NP601086.RALctX8cwb1Z_buvJK2JAoWqN7-3Ihg2l8bLsEL78xEmg130_provenance
;
np:hasPublicationInfo
dgn-np:NP601086.RALctX8cwb1Z_buvJK2JAoWqN7-3Ihg2l8bLsEL78xEmg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP601086.RALctX8cwb1Z_buvJK2JAoWqN7-3Ihg2l8bLsEL78xEmg130_assertion
a
np:Assertion
.
dgn-np:NP601086.RALctX8cwb1Z_buvJK2JAoWqN7-3Ihg2l8bLsEL78xEmg130_provenance
a
np:Provenance
.
dgn-np:NP601086.RALctX8cwb1Z_buvJK2JAoWqN7-3Ihg2l8bLsEL78xEmg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP601086.RALctX8cwb1Z_buvJK2JAoWqN7-3Ihg2l8bLsEL78xEmg130_assertion
{
miriam-gene:1543
a
ncit:C16612
.
lld:C0000786
a
ncit:C7057
.
dgn-gda:DGN14be8ec003642b3d91db043f1055029e
sio:SIO_000628
miriam-gene:1543
,
lld:C0000786
;
a
sio:SIO_001121
.
}
dgn-np:NP601086.RALctX8cwb1Z_buvJK2JAoWqN7-3Ihg2l8bLsEL78xEmg130_provenance
{
dgn-np:NP601086.RALctX8cwb1Z_buvJK2JAoWqN7-3Ihg2l8bLsEL78xEmg130_assertion
dcterms:description
"[The Ah receptor, CYP1A1, CYP1A2 and CYP1B1 genotypes were assessed in 113 Japanese women with recurrent pregnancy loss (RPL) and 203 ethnically matched women experiencing at least one live birth and no spontaneous abortion (control).]. 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:15299091
;
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:NP601086.RALctX8cwb1Z_buvJK2JAoWqN7-3Ihg2l8bLsEL78xEmg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:01+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" .
}