@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP381210.RAGRLJioZvTHR9WfB98WLCLRJF1XzrKYM0v-PTTslQ23k
> .
@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:NP381210.RAGRLJioZvTHR9WfB98WLCLRJF1XzrKYM0v-PTTslQ23k130_head
{
this:
np:hasAssertion
dgn-np:NP381210.RAGRLJioZvTHR9WfB98WLCLRJF1XzrKYM0v-PTTslQ23k130_assertion
;
np:hasProvenance
dgn-np:NP381210.RAGRLJioZvTHR9WfB98WLCLRJF1XzrKYM0v-PTTslQ23k130_provenance
;
np:hasPublicationInfo
dgn-np:NP381210.RAGRLJioZvTHR9WfB98WLCLRJF1XzrKYM0v-PTTslQ23k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP381210.RAGRLJioZvTHR9WfB98WLCLRJF1XzrKYM0v-PTTslQ23k130_assertion
a
np:Assertion
.
dgn-np:NP381210.RAGRLJioZvTHR9WfB98WLCLRJF1XzrKYM0v-PTTslQ23k130_provenance
a
np:Provenance
.
dgn-np:NP381210.RAGRLJioZvTHR9WfB98WLCLRJF1XzrKYM0v-PTTslQ23k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP381210.RAGRLJioZvTHR9WfB98WLCLRJF1XzrKYM0v-PTTslQ23k130_assertion
{
miriam-gene:5660
a
ncit:C16612
.
lld:C2584620
a
ncit:C7057
.
dgn-gda:DGN2711d6f51d48c20ce871e68f7e571af3
sio:SIO_000628
miriam-gene:5660
,
lld:C2584620
;
a
sio:SIO_001121
.
}
dgn-np:NP381210.RAGRLJioZvTHR9WfB98WLCLRJF1XzrKYM0v-PTTslQ23k130_provenance
{
dgn-np:NP381210.RAGRLJioZvTHR9WfB98WLCLRJF1XzrKYM0v-PTTslQ23k130_assertion
dcterms:description
"[These observations extend recent evidence of an increased thrombotic risk conferred by the coexistence of heterozygous PC deficiency and heterozygous activated PC resistance and support the paradigm in which hereditary thrombophilia is often a multigenic disease.]. 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:8704244
;
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:NP381210.RAGRLJioZvTHR9WfB98WLCLRJF1XzrKYM0v-PTTslQ23k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:45+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" .
}