@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP44585.RAf5An5zKsSBBgygcjgyd0aRqFHZrQ05_WkWquvVi-lco
> .
@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:NP44585.RAf5An5zKsSBBgygcjgyd0aRqFHZrQ05_WkWquvVi-lco130_head
{
this:
np:hasAssertion
dgn-np:NP44585.RAf5An5zKsSBBgygcjgyd0aRqFHZrQ05_WkWquvVi-lco130_assertion
;
np:hasProvenance
dgn-np:NP44585.RAf5An5zKsSBBgygcjgyd0aRqFHZrQ05_WkWquvVi-lco130_provenance
;
np:hasPublicationInfo
dgn-np:NP44585.RAf5An5zKsSBBgygcjgyd0aRqFHZrQ05_WkWquvVi-lco130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP44585.RAf5An5zKsSBBgygcjgyd0aRqFHZrQ05_WkWquvVi-lco130_assertion
a
np:Assertion
.
dgn-np:NP44585.RAf5An5zKsSBBgygcjgyd0aRqFHZrQ05_WkWquvVi-lco130_provenance
a
np:Provenance
.
dgn-np:NP44585.RAf5An5zKsSBBgygcjgyd0aRqFHZrQ05_WkWquvVi-lco130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP44585.RAf5An5zKsSBBgygcjgyd0aRqFHZrQ05_WkWquvVi-lco130_assertion
{
miriam-gene:2147
a
ncit:C16612
.
lld:C0000809
a
ncit:C7057
.
dgn-gda:DGN67b06aef26591c3f6bcc0a9654c5ead1
sio:SIO_000628
miriam-gene:2147
,
lld:C0000809
;
a
sio:SIO_001122
.
}
dgn-np:NP44585.RAf5An5zKsSBBgygcjgyd0aRqFHZrQ05_WkWquvVi-lco130_provenance
{
dgn-np:NP44585.RAf5An5zKsSBBgygcjgyd0aRqFHZrQ05_WkWquvVi-lco130_assertion
dcterms:description
"[Our study did not demonstrate that women who are carriers of the factor V, prothrombin, or MTHFR mutations are at higher risk of recurrent fetal loss than women without these mutations.]. 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:12380673
;
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:NP44585.RAf5An5zKsSBBgygcjgyd0aRqFHZrQ05_WkWquvVi-lco130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:20+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" .
}