@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1303723.RAxVPg_tAvxsTw1wUkSN6A0U1hNMhY-yMUBOFCoS8wk78
> .
@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:NP1303723.RAxVPg_tAvxsTw1wUkSN6A0U1hNMhY-yMUBOFCoS8wk78130_head
{
this:
np:hasAssertion
dgn-np:NP1303723.RAxVPg_tAvxsTw1wUkSN6A0U1hNMhY-yMUBOFCoS8wk78130_assertion
;
np:hasProvenance
dgn-np:NP1303723.RAxVPg_tAvxsTw1wUkSN6A0U1hNMhY-yMUBOFCoS8wk78130_provenance
;
np:hasPublicationInfo
dgn-np:NP1303723.RAxVPg_tAvxsTw1wUkSN6A0U1hNMhY-yMUBOFCoS8wk78130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1303723.RAxVPg_tAvxsTw1wUkSN6A0U1hNMhY-yMUBOFCoS8wk78130_assertion
a
np:Assertion
.
dgn-np:NP1303723.RAxVPg_tAvxsTw1wUkSN6A0U1hNMhY-yMUBOFCoS8wk78130_provenance
a
np:Provenance
.
dgn-np:NP1303723.RAxVPg_tAvxsTw1wUkSN6A0U1hNMhY-yMUBOFCoS8wk78130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1303723.RAxVPg_tAvxsTw1wUkSN6A0U1hNMhY-yMUBOFCoS8wk78130_assertion
{
miriam-gene:5554
a
ncit:C16612
.
lld:C0085650
a
ncit:C7057
.
dgn-gda:DGN3475036078928d20e56fc42380eae839
sio:SIO_000628
miriam-gene:5554
,
lld:C0085650
;
a
sio:SIO_001121
.
}
dgn-np:NP1303723.RAxVPg_tAvxsTw1wUkSN6A0U1hNMhY-yMUBOFCoS8wk78130_provenance
{
dgn-np:NP1303723.RAxVPg_tAvxsTw1wUkSN6A0U1hNMhY-yMUBOFCoS8wk78130_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-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:NP1303723.RAxVPg_tAvxsTw1wUkSN6A0U1hNMhY-yMUBOFCoS8wk78130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:37+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" .
}