@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP671407.RAmQc_Rar8SAl_Jhx-a6Mv1I0jklKmfgh578ccBosTqic
> .
@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:NP671407.RAmQc_Rar8SAl_Jhx-a6Mv1I0jklKmfgh578ccBosTqic130_head
{
this:
np:hasAssertion
dgn-np:NP671407.RAmQc_Rar8SAl_Jhx-a6Mv1I0jklKmfgh578ccBosTqic130_assertion
;
np:hasProvenance
dgn-np:NP671407.RAmQc_Rar8SAl_Jhx-a6Mv1I0jklKmfgh578ccBosTqic130_provenance
;
np:hasPublicationInfo
dgn-np:NP671407.RAmQc_Rar8SAl_Jhx-a6Mv1I0jklKmfgh578ccBosTqic130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP671407.RAmQc_Rar8SAl_Jhx-a6Mv1I0jklKmfgh578ccBosTqic130_assertion
a
np:Assertion
.
dgn-np:NP671407.RAmQc_Rar8SAl_Jhx-a6Mv1I0jklKmfgh578ccBosTqic130_provenance
a
np:Provenance
.
dgn-np:NP671407.RAmQc_Rar8SAl_Jhx-a6Mv1I0jklKmfgh578ccBosTqic130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP671407.RAmQc_Rar8SAl_Jhx-a6Mv1I0jklKmfgh578ccBosTqic130_assertion
{
miriam-gene:1326
a
ncit:C16612
.
lld:C0021670
a
ncit:C7057
.
dgn-gda:DGN61cb40b831e0e40e98d0291da57bba5a
sio:SIO_000628
miriam-gene:1326
,
lld:C0021670
;
a
sio:SIO_001121
.
}
dgn-np:NP671407.RAmQc_Rar8SAl_Jhx-a6Mv1I0jklKmfgh578ccBosTqic130_provenance
{
dgn-np:NP671407.RAmQc_Rar8SAl_Jhx-a6Mv1I0jklKmfgh578ccBosTqic130_assertion
dcterms:description
"[The results demonstrated the molecular biology of human insulinoma tissue at the level of transcript abundance and validated the efficacy of EST sequencing combined with cDNA array in the construction of gene expression profiling.]. 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:15163304
;
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:NP671407.RAmQc_Rar8SAl_Jhx-a6Mv1I0jklKmfgh578ccBosTqic130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:45+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" .
}