@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP419036.RAgIxyv0-9QBEuyx8yr8WFiBEM7Bm79X1o0BXVsr54FeM
> .
@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:NP419036.RAgIxyv0-9QBEuyx8yr8WFiBEM7Bm79X1o0BXVsr54FeM130_head
{
this:
np:hasAssertion
dgn-np:NP419036.RAgIxyv0-9QBEuyx8yr8WFiBEM7Bm79X1o0BXVsr54FeM130_assertion
;
np:hasProvenance
dgn-np:NP419036.RAgIxyv0-9QBEuyx8yr8WFiBEM7Bm79X1o0BXVsr54FeM130_provenance
;
np:hasPublicationInfo
dgn-np:NP419036.RAgIxyv0-9QBEuyx8yr8WFiBEM7Bm79X1o0BXVsr54FeM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP419036.RAgIxyv0-9QBEuyx8yr8WFiBEM7Bm79X1o0BXVsr54FeM130_assertion
a
np:Assertion
.
dgn-np:NP419036.RAgIxyv0-9QBEuyx8yr8WFiBEM7Bm79X1o0BXVsr54FeM130_provenance
a
np:Provenance
.
dgn-np:NP419036.RAgIxyv0-9QBEuyx8yr8WFiBEM7Bm79X1o0BXVsr54FeM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP419036.RAgIxyv0-9QBEuyx8yr8WFiBEM7Bm79X1o0BXVsr54FeM130_assertion
{
miriam-gene:5660
a
ncit:C16612
.
lld:C0085650
a
ncit:C7057
.
dgn-gda:DGN3505e7b93ed791ecb8b29ba368ab1f87
sio:SIO_000628
miriam-gene:5660
,
lld:C0085650
;
a
sio:SIO_001121
.
}
dgn-np:NP419036.RAgIxyv0-9QBEuyx8yr8WFiBEM7Bm79X1o0BXVsr54FeM130_provenance
{
dgn-np:NP419036.RAgIxyv0-9QBEuyx8yr8WFiBEM7Bm79X1o0BXVsr54FeM130_assertion
dcterms:description
"[Although the homozygous deficiency of protein C has been reported to be closely associated with fatal purpura fulminans or severe and massive thrombotic diseases during the neonatal period, the patient had survived the neonatal period without any clinical manifestations relevant to 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:3840289
;
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:NP419036.RAgIxyv0-9QBEuyx8yr8WFiBEM7Bm79X1o0BXVsr54FeM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:08+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" .
}