@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP291696.RAByKamG3j11ll6wHss-jvX7iYTyzYrfco1yFEF_yiGsk
> .
@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:NP291696.RAByKamG3j11ll6wHss-jvX7iYTyzYrfco1yFEF_yiGsk130_head
{
this:
np:hasAssertion
dgn-np:NP291696.RAByKamG3j11ll6wHss-jvX7iYTyzYrfco1yFEF_yiGsk130_assertion
;
np:hasProvenance
dgn-np:NP291696.RAByKamG3j11ll6wHss-jvX7iYTyzYrfco1yFEF_yiGsk130_provenance
;
np:hasPublicationInfo
dgn-np:NP291696.RAByKamG3j11ll6wHss-jvX7iYTyzYrfco1yFEF_yiGsk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP291696.RAByKamG3j11ll6wHss-jvX7iYTyzYrfco1yFEF_yiGsk130_assertion
a
np:Assertion
.
dgn-np:NP291696.RAByKamG3j11ll6wHss-jvX7iYTyzYrfco1yFEF_yiGsk130_provenance
a
np:Provenance
.
dgn-np:NP291696.RAByKamG3j11ll6wHss-jvX7iYTyzYrfco1yFEF_yiGsk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP291696.RAByKamG3j11ll6wHss-jvX7iYTyzYrfco1yFEF_yiGsk130_assertion
{
miriam-gene:5054
a
ncit:C16612
.
lld:C2827470
a
ncit:C7057
.
dgn-gda:DGNec0f55b48d22efa9bb65cb7454ec0e37
sio:SIO_000628
miriam-gene:5054
,
lld:C2827470
;
a
sio:SIO_001121
.
}
dgn-np:NP291696.RAByKamG3j11ll6wHss-jvX7iYTyzYrfco1yFEF_yiGsk130_provenance
{
dgn-np:NP291696.RAByKamG3j11ll6wHss-jvX7iYTyzYrfco1yFEF_yiGsk130_assertion
dcterms:description
"[Detailed investigations of thrombophilia showed that four patients were positive for antiphospholipid antibodies, one of whom was also homozygous for the plasminogen-activator inhibitor-1 4G/4G polymorphism, and the fifth patient was deficient for protein C. Despite the concomitant presence of both coagulation factor defect and thrombophilia, fetal loss may be attributed to factor defect that in reality is a red herring, with underlying thrombophilia not being evaluated.]. 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:17762534
;
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:NP291696.RAByKamG3j11ll6wHss-jvX7iYTyzYrfco1yFEF_yiGsk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:46+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" .
}