@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP373327.RA3IDpFNLZ_yBX3MFAx5rrNQMvnlkGGArM8EIG-2ed9EI
> .
@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:NP373327.RA3IDpFNLZ_yBX3MFAx5rrNQMvnlkGGArM8EIG-2ed9EI130_head
{
this:
np:hasAssertion
dgn-np:NP373327.RA3IDpFNLZ_yBX3MFAx5rrNQMvnlkGGArM8EIG-2ed9EI130_assertion
;
np:hasProvenance
dgn-np:NP373327.RA3IDpFNLZ_yBX3MFAx5rrNQMvnlkGGArM8EIG-2ed9EI130_provenance
;
np:hasPublicationInfo
dgn-np:NP373327.RA3IDpFNLZ_yBX3MFAx5rrNQMvnlkGGArM8EIG-2ed9EI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP373327.RA3IDpFNLZ_yBX3MFAx5rrNQMvnlkGGArM8EIG-2ed9EI130_assertion
a
np:Assertion
.
dgn-np:NP373327.RA3IDpFNLZ_yBX3MFAx5rrNQMvnlkGGArM8EIG-2ed9EI130_provenance
a
np:Provenance
.
dgn-np:NP373327.RA3IDpFNLZ_yBX3MFAx5rrNQMvnlkGGArM8EIG-2ed9EI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP373327.RA3IDpFNLZ_yBX3MFAx5rrNQMvnlkGGArM8EIG-2ed9EI130_assertion
{
miriam-gene:3133
a
ncit:C16612
.
lld:C0021359
a
ncit:C7057
.
dgn-gda:DGN03cede6bf6a206dd09244bfdd85d05c7
sio:SIO_000628
miriam-gene:3133
,
lld:C0021359
;
a
sio:SIO_001121
.
}
dgn-np:NP373327.RA3IDpFNLZ_yBX3MFAx5rrNQMvnlkGGArM8EIG-2ed9EI130_provenance
{
dgn-np:NP373327.RA3IDpFNLZ_yBX3MFAx5rrNQMvnlkGGArM8EIG-2ed9EI130_assertion
dcterms:description
"[The association between HLA sharing and recurrent spontaneous abortion (RSA) was tested in 123 couples and the association between HLA sharing, and the outcome of treatment for unexplained infertility by in vitro fertilization (IVF) was tested in 76 couples, by using a new shared-allele test in order to identify more precisely the region of the major histocompatibility complex (MHC) influencing these reproductive defects.]. 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:7762569
;
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:NP373327.RA3IDpFNLZ_yBX3MFAx5rrNQMvnlkGGArM8EIG-2ed9EI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:38+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" .
}