@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP161594.RAxjRUObSHzvF4NlOZF3lqWKChN--97fbYbM7eyG6zfv0
> .
@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:NP161594.RAxjRUObSHzvF4NlOZF3lqWKChN--97fbYbM7eyG6zfv0130_head
{
this:
np:hasAssertion
dgn-np:NP161594.RAxjRUObSHzvF4NlOZF3lqWKChN--97fbYbM7eyG6zfv0130_assertion
;
np:hasProvenance
dgn-np:NP161594.RAxjRUObSHzvF4NlOZF3lqWKChN--97fbYbM7eyG6zfv0130_provenance
;
np:hasPublicationInfo
dgn-np:NP161594.RAxjRUObSHzvF4NlOZF3lqWKChN--97fbYbM7eyG6zfv0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP161594.RAxjRUObSHzvF4NlOZF3lqWKChN--97fbYbM7eyG6zfv0130_assertion
a
np:Assertion
.
dgn-np:NP161594.RAxjRUObSHzvF4NlOZF3lqWKChN--97fbYbM7eyG6zfv0130_provenance
a
np:Provenance
.
dgn-np:NP161594.RAxjRUObSHzvF4NlOZF3lqWKChN--97fbYbM7eyG6zfv0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP161594.RAxjRUObSHzvF4NlOZF3lqWKChN--97fbYbM7eyG6zfv0130_assertion
{
miriam-gene:2153
a
ncit:C16612
.
lld:C0000786
a
ncit:C7057
.
dgn-gda:DGN3d81c38ed9726d0ca80e0ca741fa6350
sio:SIO_000628
miriam-gene:2153
,
lld:C0000786
;
a
sio:SIO_001121
.
}
dgn-np:NP161594.RAxjRUObSHzvF4NlOZF3lqWKChN--97fbYbM7eyG6zfv0130_provenance
{
dgn-np:NP161594.RAxjRUObSHzvF4NlOZF3lqWKChN--97fbYbM7eyG6zfv0130_assertion
dcterms:description
"[The objectives of the present study were to investigate the prevalence of the FVL mutation in Japanese women who have experienced RSA and to clarify the contribution of the FVL mutation to recurrent miscarriages.]. 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:10402408
;
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:NP161594.RAxjRUObSHzvF4NlOZF3lqWKChN--97fbYbM7eyG6zfv0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:27+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" .
}