@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP838371.RAga8MNLnT2fQC_BWrg3t2PcRb0JwByfGu10pa81zWjKA
> .
@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:NP838371.RAga8MNLnT2fQC_BWrg3t2PcRb0JwByfGu10pa81zWjKA130_head
{
this:
np:hasAssertion
dgn-np:NP838371.RAga8MNLnT2fQC_BWrg3t2PcRb0JwByfGu10pa81zWjKA130_assertion
;
np:hasProvenance
dgn-np:NP838371.RAga8MNLnT2fQC_BWrg3t2PcRb0JwByfGu10pa81zWjKA130_provenance
;
np:hasPublicationInfo
dgn-np:NP838371.RAga8MNLnT2fQC_BWrg3t2PcRb0JwByfGu10pa81zWjKA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP838371.RAga8MNLnT2fQC_BWrg3t2PcRb0JwByfGu10pa81zWjKA130_assertion
a
np:Assertion
.
dgn-np:NP838371.RAga8MNLnT2fQC_BWrg3t2PcRb0JwByfGu10pa81zWjKA130_provenance
a
np:Provenance
.
dgn-np:NP838371.RAga8MNLnT2fQC_BWrg3t2PcRb0JwByfGu10pa81zWjKA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP838371.RAga8MNLnT2fQC_BWrg3t2PcRb0JwByfGu10pa81zWjKA130_assertion
{
miriam-gene:7048
a
ncit:C16612
.
lld:C0238669
a
ncit:C7057
.
dgn-gda:DGN59801e36af5ce4f2a08aca2dcab70cea
sio:SIO_000628
miriam-gene:7048
,
lld:C0238669
;
a
sio:SIO_001121
.
}
dgn-np:NP838371.RAga8MNLnT2fQC_BWrg3t2PcRb0JwByfGu10pa81zWjKA130_provenance
{
dgn-np:NP838371.RAga8MNLnT2fQC_BWrg3t2PcRb0JwByfGu10pa81zWjKA130_assertion
dcterms:description
"[Genetic variants in TGFB2, TGFBR2, and SMAD3 and their haplotypes were consistently and reproducibly associated with KD susceptibility, coronary artery aneurysm formation, aortic root dilatation, and intravenous immunoglobulin treatment response in different cohorts.]. 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:21127203
;
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:NP838371.RAga8MNLnT2fQC_BWrg3t2PcRb0JwByfGu10pa81zWjKA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:32+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" .
}