@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1412817.RACP5GsITsZ5ldqgSj3qjm3hhqe0vHseXhjem2mwGEEx0
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1412817.RACP5GsITsZ5ldqgSj3qjm3hhqe0vHseXhjem2mwGEEx0130_head
{
this:
np:hasAssertion
dgn-np:NP1412817.RACP5GsITsZ5ldqgSj3qjm3hhqe0vHseXhjem2mwGEEx0130_assertion
;
np:hasProvenance
dgn-np:NP1412817.RACP5GsITsZ5ldqgSj3qjm3hhqe0vHseXhjem2mwGEEx0130_provenance
;
np:hasPublicationInfo
dgn-np:NP1412817.RACP5GsITsZ5ldqgSj3qjm3hhqe0vHseXhjem2mwGEEx0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1412817.RACP5GsITsZ5ldqgSj3qjm3hhqe0vHseXhjem2mwGEEx0130_assertion
a
np:Assertion
.
dgn-np:NP1412817.RACP5GsITsZ5ldqgSj3qjm3hhqe0vHseXhjem2mwGEEx0130_provenance
a
np:Provenance
.
dgn-np:NP1412817.RACP5GsITsZ5ldqgSj3qjm3hhqe0vHseXhjem2mwGEEx0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1412817.RACP5GsITsZ5ldqgSj3qjm3hhqe0vHseXhjem2mwGEEx0130_assertion
{
miriam-gene:2147
a
ncit:C16612
.
lld:C0948008
a
ncit:C7057
.
dgn-gda:DGN0e37dc15db48c08a1e9af66479f7530e
sio:SIO_000628
miriam-gene:2147
,
lld:C0948008
;
a
sio:SIO_001121
.
}
dgn-np:NP1412817.RACP5GsITsZ5ldqgSj3qjm3hhqe0vHseXhjem2mwGEEx0130_provenance
{
dgn-np:NP1412817.RACP5GsITsZ5ldqgSj3qjm3hhqe0vHseXhjem2mwGEEx0130_assertion
dcterms:description
"[In view of recent reports of an increased risk for ischemic cerebral vascular disease in patients with the prothrombin 20210A mutation, we suggest that many of the reported cases of ischemic stroke and protein C deficiency may have had additional prothrombotic disorders such as the prothrombin mutation.]. 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:9890720
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1412817.RACP5GsITsZ5ldqgSj3qjm3hhqe0vHseXhjem2mwGEEx0130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:27+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}