@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP813942.RA68aSyjKhVQo-Aln3UARnOsqN59F5eUvykgyd_77Fc3I
> .
@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:NP813942.RA68aSyjKhVQo-Aln3UARnOsqN59F5eUvykgyd_77Fc3I130_head
{
this:
np:hasAssertion
dgn-np:NP813942.RA68aSyjKhVQo-Aln3UARnOsqN59F5eUvykgyd_77Fc3I130_assertion
;
np:hasProvenance
dgn-np:NP813942.RA68aSyjKhVQo-Aln3UARnOsqN59F5eUvykgyd_77Fc3I130_provenance
;
np:hasPublicationInfo
dgn-np:NP813942.RA68aSyjKhVQo-Aln3UARnOsqN59F5eUvykgyd_77Fc3I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP813942.RA68aSyjKhVQo-Aln3UARnOsqN59F5eUvykgyd_77Fc3I130_assertion
a
np:Assertion
.
dgn-np:NP813942.RA68aSyjKhVQo-Aln3UARnOsqN59F5eUvykgyd_77Fc3I130_provenance
a
np:Provenance
.
dgn-np:NP813942.RA68aSyjKhVQo-Aln3UARnOsqN59F5eUvykgyd_77Fc3I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP813942.RA68aSyjKhVQo-Aln3UARnOsqN59F5eUvykgyd_77Fc3I130_assertion
{
miriam-gene:54808
a
ncit:C16612
.
lld:C0042373
a
ncit:C7057
.
dgn-gda:DGNa673453c5873415ba8262c4cef2f44be
sio:SIO_000628
miriam-gene:54808
,
lld:C0042373
;
a
sio:SIO_001121
.
}
dgn-np:NP813942.RA68aSyjKhVQo-Aln3UARnOsqN59F5eUvykgyd_77Fc3I130_provenance
{
dgn-np:NP813942.RA68aSyjKhVQo-Aln3UARnOsqN59F5eUvykgyd_77Fc3I130_assertion
dcterms:description
"[Using the myosin isoform approach to study vascular SMC biology, we have shown (1) a marked SMC heterogeneity in adult arterial vessels, ie, coexistence of an `immature` and a fully differentiated SMC population; and (2) the propensity of the immature type SMC population to be activated in experimental models and human vascular diseases that are characterized by proliferation and migration of medial SMCs into the subendothelial space.]. 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:9261248
;
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:NP813942.RA68aSyjKhVQo-Aln3UARnOsqN59F5eUvykgyd_77Fc3I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:19+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" .
}