@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP839512.RAump7xMBn862b4rYrPTZ09L5Fe1pRAkh15iCU-S0W2nY
> .
@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:NP839512.RAump7xMBn862b4rYrPTZ09L5Fe1pRAkh15iCU-S0W2nY130_head
{
this:
np:hasAssertion
dgn-np:NP839512.RAump7xMBn862b4rYrPTZ09L5Fe1pRAkh15iCU-S0W2nY130_assertion
;
np:hasProvenance
dgn-np:NP839512.RAump7xMBn862b4rYrPTZ09L5Fe1pRAkh15iCU-S0W2nY130_provenance
;
np:hasPublicationInfo
dgn-np:NP839512.RAump7xMBn862b4rYrPTZ09L5Fe1pRAkh15iCU-S0W2nY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP839512.RAump7xMBn862b4rYrPTZ09L5Fe1pRAkh15iCU-S0W2nY130_assertion
a
np:Assertion
.
dgn-np:NP839512.RAump7xMBn862b4rYrPTZ09L5Fe1pRAkh15iCU-S0W2nY130_provenance
a
np:Provenance
.
dgn-np:NP839512.RAump7xMBn862b4rYrPTZ09L5Fe1pRAkh15iCU-S0W2nY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP839512.RAump7xMBn862b4rYrPTZ09L5Fe1pRAkh15iCU-S0W2nY130_assertion
{
miriam-gene:4221
a
ncit:C16612
.
lld:C0027627
a
ncit:C7057
.
dgn-gda:DGNbd485af79c4a53511a508a07d1239b01
sio:SIO_000628
miriam-gene:4221
,
lld:C0027627
;
a
sio:SIO_001121
.
}
dgn-np:NP839512.RAump7xMBn862b4rYrPTZ09L5Fe1pRAkh15iCU-S0W2nY130_provenance
{
dgn-np:NP839512.RAump7xMBn862b4rYrPTZ09L5Fe1pRAkh15iCU-S0W2nY130_assertion
dcterms:description
"[We used tissue microdissection to analyze 95 archival pancreatic and duodenal ETs and metastases from 50 patients for loss of heterozygosity (LOH) on 11q13 with 10 polymorphic markers spanning the area of the putative MEN1 gene.]. 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:9187127
;
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:NP839512.RAump7xMBn862b4rYrPTZ09L5Fe1pRAkh15iCU-S0W2nY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:33+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" .
}