@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP296525.RA3tZXQiyMo4Zf0DxKf5k5LK4i1TvkOwH89JJZ-70hT78
> .
@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:NP296525.RA3tZXQiyMo4Zf0DxKf5k5LK4i1TvkOwH89JJZ-70hT78130_head
{
this:
np:hasAssertion
dgn-np:NP296525.RA3tZXQiyMo4Zf0DxKf5k5LK4i1TvkOwH89JJZ-70hT78130_assertion
;
np:hasProvenance
dgn-np:NP296525.RA3tZXQiyMo4Zf0DxKf5k5LK4i1TvkOwH89JJZ-70hT78130_provenance
;
np:hasPublicationInfo
dgn-np:NP296525.RA3tZXQiyMo4Zf0DxKf5k5LK4i1TvkOwH89JJZ-70hT78130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP296525.RA3tZXQiyMo4Zf0DxKf5k5LK4i1TvkOwH89JJZ-70hT78130_assertion
a
np:Assertion
.
dgn-np:NP296525.RA3tZXQiyMo4Zf0DxKf5k5LK4i1TvkOwH89JJZ-70hT78130_provenance
a
np:Provenance
.
dgn-np:NP296525.RA3tZXQiyMo4Zf0DxKf5k5LK4i1TvkOwH89JJZ-70hT78130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP296525.RA3tZXQiyMo4Zf0DxKf5k5LK4i1TvkOwH89JJZ-70hT78130_assertion
{
miriam-gene:4210
a
ncit:C16612
.
lld:C0027651
a
ncit:C7057
.
dgn-gda:DGN3b94aa82705251031fa832dc8f6f08fa
sio:SIO_000628
miriam-gene:4210
,
lld:C0027651
;
a
sio:SIO_001121
.
}
dgn-np:NP296525.RA3tZXQiyMo4Zf0DxKf5k5LK4i1TvkOwH89JJZ-70hT78130_provenance
{
dgn-np:NP296525.RA3tZXQiyMo4Zf0DxKf5k5LK4i1TvkOwH89JJZ-70hT78130_assertion
dcterms:description
"[Although no single underlying defect could be targeted in all hematologic neoplasms, it will be important to fully exploit the mechanisms underlying the neoplasm promoting role of inherited variants in MEFV.]. 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:22453916
;
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:NP296525.RA3tZXQiyMo4Zf0DxKf5k5LK4i1TvkOwH89JJZ-70hT78130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:48+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: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" .
}