@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP294767.RAIU8tlVSjhiMTQIbqMQj4biDc8mTV6puSNGMPoQuEI5o
> .
@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:NP294767.RAIU8tlVSjhiMTQIbqMQj4biDc8mTV6puSNGMPoQuEI5o130_head
{
this:
np:hasAssertion
dgn-np:NP294767.RAIU8tlVSjhiMTQIbqMQj4biDc8mTV6puSNGMPoQuEI5o130_assertion
;
np:hasProvenance
dgn-np:NP294767.RAIU8tlVSjhiMTQIbqMQj4biDc8mTV6puSNGMPoQuEI5o130_provenance
;
np:hasPublicationInfo
dgn-np:NP294767.RAIU8tlVSjhiMTQIbqMQj4biDc8mTV6puSNGMPoQuEI5o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP294767.RAIU8tlVSjhiMTQIbqMQj4biDc8mTV6puSNGMPoQuEI5o130_assertion
a
np:Assertion
.
dgn-np:NP294767.RAIU8tlVSjhiMTQIbqMQj4biDc8mTV6puSNGMPoQuEI5o130_provenance
a
np:Provenance
.
dgn-np:NP294767.RAIU8tlVSjhiMTQIbqMQj4biDc8mTV6puSNGMPoQuEI5o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP294767.RAIU8tlVSjhiMTQIbqMQj4biDc8mTV6puSNGMPoQuEI5o130_assertion
{
miriam-gene:5660
a
ncit:C16612
.
lld:C0584960
a
ncit:C7057
.
dgn-gda:DGN668d6b390cc961d2a8c9d15367fca890
sio:SIO_000628
miriam-gene:5660
,
lld:C0584960
;
a
sio:SIO_001121
.
}
dgn-np:NP294767.RAIU8tlVSjhiMTQIbqMQj4biDc8mTV6puSNGMPoQuEI5o130_provenance
{
dgn-np:NP294767.RAIU8tlVSjhiMTQIbqMQj4biDc8mTV6puSNGMPoQuEI5o130_assertion
dcterms:description
"[Risks for venous thromboembolism in genetically affected persons are substantially higher among patients with coexistent predispositions for thrombosis, such as advanced age, use of oral contraceptives, hyperhomocystinemia, and deficiencies of protein C and protein S. Factor V Leiden mutation does not seem to increase risks for arterial thrombosis.]. 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:9382368
;
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:NP294767.RAIU8tlVSjhiMTQIbqMQj4biDc8mTV6puSNGMPoQuEI5o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:47+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" .
}