@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP622818.RAkf5qVwreqmhRoLXgqtF_B69tGyir6NW_H2zILPiZ_zo
> .
@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:NP622818.RAkf5qVwreqmhRoLXgqtF_B69tGyir6NW_H2zILPiZ_zo130_head
{
this:
np:hasAssertion
dgn-np:NP622818.RAkf5qVwreqmhRoLXgqtF_B69tGyir6NW_H2zILPiZ_zo130_assertion
;
np:hasProvenance
dgn-np:NP622818.RAkf5qVwreqmhRoLXgqtF_B69tGyir6NW_H2zILPiZ_zo130_provenance
;
np:hasPublicationInfo
dgn-np:NP622818.RAkf5qVwreqmhRoLXgqtF_B69tGyir6NW_H2zILPiZ_zo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP622818.RAkf5qVwreqmhRoLXgqtF_B69tGyir6NW_H2zILPiZ_zo130_assertion
a
np:Assertion
.
dgn-np:NP622818.RAkf5qVwreqmhRoLXgqtF_B69tGyir6NW_H2zILPiZ_zo130_provenance
a
np:Provenance
.
dgn-np:NP622818.RAkf5qVwreqmhRoLXgqtF_B69tGyir6NW_H2zILPiZ_zo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP622818.RAkf5qVwreqmhRoLXgqtF_B69tGyir6NW_H2zILPiZ_zo130_assertion
{
miriam-gene:3133
a
ncit:C16612
.
lld:C0699893
a
ncit:C7057
.
dgn-gda:DGN478436139355e48fd51de6a8110a2228
sio:SIO_000628
miriam-gene:3133
,
lld:C0699893
;
a
sio:SIO_001121
.
}
dgn-np:NP622818.RAkf5qVwreqmhRoLXgqtF_B69tGyir6NW_H2zILPiZ_zo130_provenance
{
dgn-np:NP622818.RAkf5qVwreqmhRoLXgqtF_B69tGyir6NW_H2zILPiZ_zo130_assertion
dcterms:description
"[Here, we have extended the previous microsatellite study by using the same DNA samples obtained from 154 NMSC patients and 213 normal controls from the town of Busselton in Western Australia and examined the relationship between five polymorphic Alu insertions (POALINs) within the MHC class I region and their association with NMSC.]. 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:16866882
;
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:NP622818.RAkf5qVwreqmhRoLXgqtF_B69tGyir6NW_H2zILPiZ_zo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:16+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" .
}