@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP44485.RAgDuychGRJyP0Uu6K9UyqEuEMRYetWxgt04qrDQjqA5Y
> .
@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 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:NP44485.RAgDuychGRJyP0Uu6K9UyqEuEMRYetWxgt04qrDQjqA5Y130_head
{
this:
np:hasAssertion
dgn-np:NP44485.RAgDuychGRJyP0Uu6K9UyqEuEMRYetWxgt04qrDQjqA5Y130_assertion
;
np:hasProvenance
dgn-np:NP44485.RAgDuychGRJyP0Uu6K9UyqEuEMRYetWxgt04qrDQjqA5Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP44485.RAgDuychGRJyP0Uu6K9UyqEuEMRYetWxgt04qrDQjqA5Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP44485.RAgDuychGRJyP0Uu6K9UyqEuEMRYetWxgt04qrDQjqA5Y130_assertion
a
np:Assertion
.
dgn-np:NP44485.RAgDuychGRJyP0Uu6K9UyqEuEMRYetWxgt04qrDQjqA5Y130_provenance
a
np:Provenance
.
dgn-np:NP44485.RAgDuychGRJyP0Uu6K9UyqEuEMRYetWxgt04qrDQjqA5Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP44485.RAgDuychGRJyP0Uu6K9UyqEuEMRYetWxgt04qrDQjqA5Y130_assertion
{
miriam-gene:2153
a
ncit:C16612
.
lld:C0000809
a
ncit:C7057
.
dgn-gda:DGN8f2e96970a1055441f12509af5bae44f
sio:SIO_000628
miriam-gene:2153
,
lld:C0000809
;
a
sio:SIO_001122
.
}
dgn-np:NP44485.RAgDuychGRJyP0Uu6K9UyqEuEMRYetWxgt04qrDQjqA5Y130_provenance
{
dgn-np:NP44485.RAgDuychGRJyP0Uu6K9UyqEuEMRYetWxgt04qrDQjqA5Y130_assertion
dct: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:NP44485.RAgDuychGRJyP0Uu6K9UyqEuEMRYetWxgt04qrDQjqA5Y130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:20+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}