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http://rdf.disgenet.org/nanopublications.trig#NP643243.RAjCQC6HlIsob102ZbBu9VBDysp8kAFhmKGu8YgYNXFlg
> .
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http://www.w3.org/2000/01/rdf-schema#
> .
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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#
> .
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http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
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{
this:
np:hasAssertion
dgn-np:NP643243.RAjCQC6HlIsob102ZbBu9VBDysp8kAFhmKGu8YgYNXFlg130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP643243.RAjCQC6HlIsob102ZbBu9VBDysp8kAFhmKGu8YgYNXFlg130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP643243.RAjCQC6HlIsob102ZbBu9VBDysp8kAFhmKGu8YgYNXFlg130_assertion
a
np:Assertion
.
dgn-np:NP643243.RAjCQC6HlIsob102ZbBu9VBDysp8kAFhmKGu8YgYNXFlg130_provenance
a
np:Provenance
.
dgn-np:NP643243.RAjCQC6HlIsob102ZbBu9VBDysp8kAFhmKGu8YgYNXFlg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP643243.RAjCQC6HlIsob102ZbBu9VBDysp8kAFhmKGu8YgYNXFlg130_assertion
{
miriam-gene:59
a
ncit:C16612
.
lld:C0024796
a
ncit:C7057
.
dgn-gda:DGN9cf1c517fb68f0672c4da6101c547200
sio:SIO_000628
miriam-gene:59
,
lld:C0024796
;
a
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.
}
dgn-np:NP643243.RAjCQC6HlIsob102ZbBu9VBDysp8kAFhmKGu8YgYNXFlg130_provenance
{
dgn-np:NP643243.RAjCQC6HlIsob102ZbBu9VBDysp8kAFhmKGu8YgYNXFlg130_assertion
dcterms:description
"[In order to further explore the role of ACTA2 variations in the pathogenesis of TAAD, we sequenced the coding regions of this gene in 40 unrelated German patients with TAAD (with (n=21) or without (n=19) clinical features suggestive of Marfan 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:21248741
;
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 .
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dgn-np:NP643243.RAjCQC6HlIsob102ZbBu9VBDysp8kAFhmKGu8YgYNXFlg130_publicationInfo
{
this:
dcterms:created
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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
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> , <
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> , <
http://orcid.org/0000-0002-9383-528X
> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
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> ;
pav:version
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