@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP158379.RAQNWC0gZMvQCCDtY588-6nHefmScj8rZd6jX39ZQrx4k
> .
@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:NP158379.RAQNWC0gZMvQCCDtY588-6nHefmScj8rZd6jX39ZQrx4k130_head
{
this:
np:hasAssertion
dgn-np:NP158379.RAQNWC0gZMvQCCDtY588-6nHefmScj8rZd6jX39ZQrx4k130_assertion
;
np:hasProvenance
dgn-np:NP158379.RAQNWC0gZMvQCCDtY588-6nHefmScj8rZd6jX39ZQrx4k130_provenance
;
np:hasPublicationInfo
dgn-np:NP158379.RAQNWC0gZMvQCCDtY588-6nHefmScj8rZd6jX39ZQrx4k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP158379.RAQNWC0gZMvQCCDtY588-6nHefmScj8rZd6jX39ZQrx4k130_assertion
a
np:Assertion
.
dgn-np:NP158379.RAQNWC0gZMvQCCDtY588-6nHefmScj8rZd6jX39ZQrx4k130_provenance
a
np:Provenance
.
dgn-np:NP158379.RAQNWC0gZMvQCCDtY588-6nHefmScj8rZd6jX39ZQrx4k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP158379.RAQNWC0gZMvQCCDtY588-6nHefmScj8rZd6jX39ZQrx4k130_assertion
{
miriam-gene:7132
a
ncit:C16612
.
lld:C0243050
a
ncit:C7057
.
dgn-gda:DGNb2bc7899f8ca08af5b9944b50c1cb044
sio:SIO_000628
miriam-gene:7132
,
lld:C0243050
;
a
sio:SIO_001121
.
}
dgn-np:NP158379.RAQNWC0gZMvQCCDtY588-6nHefmScj8rZd6jX39ZQrx4k130_provenance
{
dgn-np:NP158379.RAQNWC0gZMvQCCDtY588-6nHefmScj8rZd6jX39ZQrx4k130_assertion
dcterms:description
"[Pericardial diseases are the most represented cardiovascular abnormalities, though the role of MEFV and TNFRSF1A in the initiation of heart involvement has not been demonstrated formally and will be discussed herein.]. 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:21284530
;
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:NP158379.RAQNWC0gZMvQCCDtY588-6nHefmScj8rZd6jX39ZQrx4k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:25+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" .
}