@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP354388.RA-pHymdMzejW6Ms985IpLKzFAclTWY2zpvJxpq948AQ8
> .
@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:NP354388.RA-pHymdMzejW6Ms985IpLKzFAclTWY2zpvJxpq948AQ8130_head
{
this:
np:hasAssertion
dgn-np:NP354388.RA-pHymdMzejW6Ms985IpLKzFAclTWY2zpvJxpq948AQ8130_assertion
;
np:hasProvenance
dgn-np:NP354388.RA-pHymdMzejW6Ms985IpLKzFAclTWY2zpvJxpq948AQ8130_provenance
;
np:hasPublicationInfo
dgn-np:NP354388.RA-pHymdMzejW6Ms985IpLKzFAclTWY2zpvJxpq948AQ8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP354388.RA-pHymdMzejW6Ms985IpLKzFAclTWY2zpvJxpq948AQ8130_assertion
a
np:Assertion
.
dgn-np:NP354388.RA-pHymdMzejW6Ms985IpLKzFAclTWY2zpvJxpq948AQ8130_provenance
a
np:Provenance
.
dgn-np:NP354388.RA-pHymdMzejW6Ms985IpLKzFAclTWY2zpvJxpq948AQ8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP354388.RA-pHymdMzejW6Ms985IpLKzFAclTWY2zpvJxpq948AQ8130_assertion
{
miriam-gene:59
a
ncit:C16612
.
lld:C0026654
a
ncit:C7057
.
dgn-gda:DGNb823a3fd0d7eec0e1be02fdca00cf1f9
sio:SIO_000628
miriam-gene:59
,
lld:C0026654
;
a
sio:SIO_001121
.
}
dgn-np:NP354388.RA-pHymdMzejW6Ms985IpLKzFAclTWY2zpvJxpq948AQ8130_provenance
{
dgn-np:NP354388.RA-pHymdMzejW6Ms985IpLKzFAclTWY2zpvJxpq948AQ8130_assertion
dcterms:description
"[DNA sequencing of the nine exons and flanking intronic regions of ACTA2 was performed in 39 MMD patients with no family history for MMD or TAAD and 68 healthy controls of central European descent with custom made primers.]. 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:20970362
;
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:NP354388.RA-pHymdMzejW6Ms985IpLKzFAclTWY2zpvJxpq948AQ8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:28+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" .
}