@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP215083.RAZMRILzLXZF5k0fniM8eo6Cp0946O8tv6NaoQDRllCwQ
> .
@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:NP215083.RAZMRILzLXZF5k0fniM8eo6Cp0946O8tv6NaoQDRllCwQ130_head
{
this:
np:hasAssertion
dgn-np:NP215083.RAZMRILzLXZF5k0fniM8eo6Cp0946O8tv6NaoQDRllCwQ130_assertion
;
np:hasProvenance
dgn-np:NP215083.RAZMRILzLXZF5k0fniM8eo6Cp0946O8tv6NaoQDRllCwQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP215083.RAZMRILzLXZF5k0fniM8eo6Cp0946O8tv6NaoQDRllCwQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP215083.RAZMRILzLXZF5k0fniM8eo6Cp0946O8tv6NaoQDRllCwQ130_assertion
a
np:Assertion
.
dgn-np:NP215083.RAZMRILzLXZF5k0fniM8eo6Cp0946O8tv6NaoQDRllCwQ130_provenance
a
np:Provenance
.
dgn-np:NP215083.RAZMRILzLXZF5k0fniM8eo6Cp0946O8tv6NaoQDRllCwQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP215083.RAZMRILzLXZF5k0fniM8eo6Cp0946O8tv6NaoQDRllCwQ130_assertion
{
miriam-gene:8170
a
ncit:C16612
.
lld:C0026769
a
ncit:C7057
.
dgn-gda:DGN8f76d7b0716923e0277a160d95f03b14
sio:SIO_000628
miriam-gene:8170
,
lld:C0026769
;
a
sio:SIO_001121
.
}
dgn-np:NP215083.RAZMRILzLXZF5k0fniM8eo6Cp0946O8tv6NaoQDRllCwQ130_provenance
{
dgn-np:NP215083.RAZMRILzLXZF5k0fniM8eo6Cp0946O8tv6NaoQDRllCwQ130_assertion
dcterms:description
"[In the second stage of the study, we resequenced the exons and the 3' untranslated (UTR) region of ACCN1, and investigated the MS association of Single Nucleotide Polymorphisms (SNPs) identified in that region.]. 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:17534430
;
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:NP215083.RAZMRILzLXZF5k0fniM8eo6Cp0946O8tv6NaoQDRllCwQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:59+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" .
}