@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP616683.RAGnQyGIln9DPP3Xrwkzcni6C36YunVwGjDr2zW2v2SIc
> .
@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/v3.0.0/void/
> .
dgn-np:NP616683.RAGnQyGIln9DPP3Xrwkzcni6C36YunVwGjDr2zW2v2SIc130_head
{
this:
np:hasAssertion
dgn-np:NP616683.RAGnQyGIln9DPP3Xrwkzcni6C36YunVwGjDr2zW2v2SIc130_assertion
;
np:hasProvenance
dgn-np:NP616683.RAGnQyGIln9DPP3Xrwkzcni6C36YunVwGjDr2zW2v2SIc130_provenance
;
np:hasPublicationInfo
dgn-np:NP616683.RAGnQyGIln9DPP3Xrwkzcni6C36YunVwGjDr2zW2v2SIc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP616683.RAGnQyGIln9DPP3Xrwkzcni6C36YunVwGjDr2zW2v2SIc130_assertion
a
np:Assertion
.
dgn-np:NP616683.RAGnQyGIln9DPP3Xrwkzcni6C36YunVwGjDr2zW2v2SIc130_provenance
a
np:Provenance
.
dgn-np:NP616683.RAGnQyGIln9DPP3Xrwkzcni6C36YunVwGjDr2zW2v2SIc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP616683.RAGnQyGIln9DPP3Xrwkzcni6C36YunVwGjDr2zW2v2SIc130_assertion
{
miriam-gene:5216
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN9b7bf752f8489f247ad91144edb51a3c
sio:SIO_000628
miriam-gene:5216
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP616683.RAGnQyGIln9DPP3Xrwkzcni6C36YunVwGjDr2zW2v2SIc130_provenance
{
dgn-np:NP616683.RAGnQyGIln9DPP3Xrwkzcni6C36YunVwGjDr2zW2v2SIc130_assertion
dcterms:description
"[As discussed in this chapter, deficiency of PFN due to the mutations of its gene, PFN1, can be associated with malignancies and severe immune disorders such as familial hemophagocytic lymphohistiocytosis (FHL) and macrophage activation syndrome.]. 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:24798014
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP616683.RAGnQyGIln9DPP3Xrwkzcni6C36YunVwGjDr2zW2v2SIc130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:43:48+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}