@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP741837.RAQGpoCtECya12zLeDzyDVoZLuvXeu0usyg-Ep03iEh2g
> .
@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:NP741837.RAQGpoCtECya12zLeDzyDVoZLuvXeu0usyg-Ep03iEh2g130_head
{
this:
np:hasAssertion
dgn-np:NP741837.RAQGpoCtECya12zLeDzyDVoZLuvXeu0usyg-Ep03iEh2g130_assertion
;
np:hasProvenance
dgn-np:NP741837.RAQGpoCtECya12zLeDzyDVoZLuvXeu0usyg-Ep03iEh2g130_provenance
;
np:hasPublicationInfo
dgn-np:NP741837.RAQGpoCtECya12zLeDzyDVoZLuvXeu0usyg-Ep03iEh2g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP741837.RAQGpoCtECya12zLeDzyDVoZLuvXeu0usyg-Ep03iEh2g130_assertion
a
np:Assertion
.
dgn-np:NP741837.RAQGpoCtECya12zLeDzyDVoZLuvXeu0usyg-Ep03iEh2g130_provenance
a
np:Provenance
.
dgn-np:NP741837.RAQGpoCtECya12zLeDzyDVoZLuvXeu0usyg-Ep03iEh2g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP741837.RAQGpoCtECya12zLeDzyDVoZLuvXeu0usyg-Ep03iEh2g130_assertion
{
miriam-gene:2099
a
ncit:C16612
.
lld:C0000786
a
ncit:C7057
.
dgn-gda:DGN7983c58e0ee59fd17af4e940d69c072a
sio:SIO_000628
miriam-gene:2099
,
lld:C0000786
;
a
sio:SIO_001121
.
}
dgn-np:NP741837.RAQGpoCtECya12zLeDzyDVoZLuvXeu0usyg-Ep03iEh2g130_provenance
{
dgn-np:NP741837.RAQGpoCtECya12zLeDzyDVoZLuvXeu0usyg-Ep03iEh2g130_assertion
dcterms:description
"[The frequency of the estrogen receptor gene variant in blood lymphocyte deoxyribonucleic acid and other selected maternal characteristics was compared among 60 primary recurrent aborters, 61 secondary recurrent aborters, and 43 women who had had at least two live births but no spontaneous abortions.]. 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:7802071
;
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:NP741837.RAQGpoCtECya12zLeDzyDVoZLuvXeu0usyg-Ep03iEh2g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:30+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" .
}