@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP449885.RACcQOsPAYnEsLv-BAakKDl2wFOMHmriDSC0dLrcU45eM
> .
@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:NP449885.RACcQOsPAYnEsLv-BAakKDl2wFOMHmriDSC0dLrcU45eM130_head
{
this:
np:hasAssertion
dgn-np:NP449885.RACcQOsPAYnEsLv-BAakKDl2wFOMHmriDSC0dLrcU45eM130_assertion
;
np:hasProvenance
dgn-np:NP449885.RACcQOsPAYnEsLv-BAakKDl2wFOMHmriDSC0dLrcU45eM130_provenance
;
np:hasPublicationInfo
dgn-np:NP449885.RACcQOsPAYnEsLv-BAakKDl2wFOMHmriDSC0dLrcU45eM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP449885.RACcQOsPAYnEsLv-BAakKDl2wFOMHmriDSC0dLrcU45eM130_assertion
a
np:Assertion
.
dgn-np:NP449885.RACcQOsPAYnEsLv-BAakKDl2wFOMHmriDSC0dLrcU45eM130_provenance
a
np:Provenance
.
dgn-np:NP449885.RACcQOsPAYnEsLv-BAakKDl2wFOMHmriDSC0dLrcU45eM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP449885.RACcQOsPAYnEsLv-BAakKDl2wFOMHmriDSC0dLrcU45eM130_assertion
{
miriam-gene:4638
a
ncit:C16612
.
lld:C1290884
a
ncit:C7057
.
dgn-gda:DGNe0d32d4b5b94b8d69e1fc07466372098
sio:SIO_000628
miriam-gene:4638
,
lld:C1290884
;
a
sio:SIO_001121
.
}
dgn-np:NP449885.RACcQOsPAYnEsLv-BAakKDl2wFOMHmriDSC0dLrcU45eM130_provenance
{
dgn-np:NP449885.RACcQOsPAYnEsLv-BAakKDl2wFOMHmriDSC0dLrcU45eM130_assertion
dcterms:description
"[These functional insights into the involvement of intronic MYLK SNPs further strengthen the concept that MYLK contributes to inflammatory disease susceptibility and represents an attractive molecular target in complex inflammatory disorders.]. 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:22015949
;
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:NP449885.RACcQOsPAYnEsLv-BAakKDl2wFOMHmriDSC0dLrcU45eM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:28+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" .
}