@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP700610.RAKTuoWkBePe4jrQ-dUB5w3Yn8gEI3ctSBhvgZLRPT1zY
> .
@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:NP700610.RAKTuoWkBePe4jrQ-dUB5w3Yn8gEI3ctSBhvgZLRPT1zY130_head
{
this:
np:hasAssertion
dgn-np:NP700610.RAKTuoWkBePe4jrQ-dUB5w3Yn8gEI3ctSBhvgZLRPT1zY130_assertion
;
np:hasProvenance
dgn-np:NP700610.RAKTuoWkBePe4jrQ-dUB5w3Yn8gEI3ctSBhvgZLRPT1zY130_provenance
;
np:hasPublicationInfo
dgn-np:NP700610.RAKTuoWkBePe4jrQ-dUB5w3Yn8gEI3ctSBhvgZLRPT1zY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP700610.RAKTuoWkBePe4jrQ-dUB5w3Yn8gEI3ctSBhvgZLRPT1zY130_assertion
a
np:Assertion
.
dgn-np:NP700610.RAKTuoWkBePe4jrQ-dUB5w3Yn8gEI3ctSBhvgZLRPT1zY130_provenance
a
np:Provenance
.
dgn-np:NP700610.RAKTuoWkBePe4jrQ-dUB5w3Yn8gEI3ctSBhvgZLRPT1zY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP700610.RAKTuoWkBePe4jrQ-dUB5w3Yn8gEI3ctSBhvgZLRPT1zY130_assertion
{
miriam-gene:2147
a
ncit:C16612
.
lld:C0398625
a
ncit:C7057
.
dgn-gda:DGN0193f5738cbd854e1099202ac7476b70
sio:SIO_000628
miriam-gene:2147
,
lld:C0398625
;
a
sio:SIO_001121
.
}
dgn-np:NP700610.RAKTuoWkBePe4jrQ-dUB5w3Yn8gEI3ctSBhvgZLRPT1zY130_provenance
{
dgn-np:NP700610.RAKTuoWkBePe4jrQ-dUB5w3Yn8gEI3ctSBhvgZLRPT1zY130_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-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:NP700610.RAKTuoWkBePe4jrQ-dUB5w3Yn8gEI3ctSBhvgZLRPT1zY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:06+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" .
}