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http://rdf.disgenet.org/nanopublications.trig#NP802080.RAP24KgfvXKZNh7iLCK2DFVMydzYuvAoyLevpHmSXYFUM
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
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http://www.w3.org/2001/XMLSchema#
> .
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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#
> .
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{
this:
np:hasAssertion
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np:hasProvenance
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dgn-np:NP802080.RAP24KgfvXKZNh7iLCK2DFVMydzYuvAoyLevpHmSXYFUM130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP802080.RAP24KgfvXKZNh7iLCK2DFVMydzYuvAoyLevpHmSXYFUM130_assertion
a
np:Assertion
.
dgn-np:NP802080.RAP24KgfvXKZNh7iLCK2DFVMydzYuvAoyLevpHmSXYFUM130_provenance
a
np:Provenance
.
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np:PublicationInfo
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{
miriam-gene:6722
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGN285bbb65f4ef62ac28429d2980a38da5
sio:SIO_000628
miriam-gene:6722
,
lld:C0002395
;
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.
}
dgn-np:NP802080.RAP24KgfvXKZNh7iLCK2DFVMydzYuvAoyLevpHmSXYFUM130_provenance
{
dgn-np:NP802080.RAP24KgfvXKZNh7iLCK2DFVMydzYuvAoyLevpHmSXYFUM130_assertion
dcterms:description
"[We report vascular smooth muscle cells (VSMC) in small pial and intracerebral arteries, which are critical for CBF regulation, express in AD high levels of serum response factor (SRF) and myocardin (MYOCD), two interacting transcription factors that orchestrate a VSMC-differentiated phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:17215356
;
prov:wasDerivedFrom
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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:NP802080.RAP24KgfvXKZNh7iLCK2DFVMydzYuvAoyLevpHmSXYFUM130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
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http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
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> , <
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> , <
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> ;
pav:createdBy
<
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