@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP618868.RADr4kCQMMt_uDmlFSwaT4XsKS3lg_dEDl2lNCX10LDyk
> .
@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:NP618868.RADr4kCQMMt_uDmlFSwaT4XsKS3lg_dEDl2lNCX10LDyk130_head
{
this:
np:hasAssertion
dgn-np:NP618868.RADr4kCQMMt_uDmlFSwaT4XsKS3lg_dEDl2lNCX10LDyk130_assertion
;
np:hasProvenance
dgn-np:NP618868.RADr4kCQMMt_uDmlFSwaT4XsKS3lg_dEDl2lNCX10LDyk130_provenance
;
np:hasPublicationInfo
dgn-np:NP618868.RADr4kCQMMt_uDmlFSwaT4XsKS3lg_dEDl2lNCX10LDyk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP618868.RADr4kCQMMt_uDmlFSwaT4XsKS3lg_dEDl2lNCX10LDyk130_assertion
a
np:Assertion
.
dgn-np:NP618868.RADr4kCQMMt_uDmlFSwaT4XsKS3lg_dEDl2lNCX10LDyk130_provenance
a
np:Provenance
.
dgn-np:NP618868.RADr4kCQMMt_uDmlFSwaT4XsKS3lg_dEDl2lNCX10LDyk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP618868.RADr4kCQMMt_uDmlFSwaT4XsKS3lg_dEDl2lNCX10LDyk130_assertion
{
miriam-gene:3133
a
ncit:C16612
.
lld:C0263214
a
ncit:C7057
.
dgn-gda:DGNae371b9f84b5601c80b1ea3671b18254
sio:SIO_000628
miriam-gene:3133
,
lld:C0263214
;
a
sio:SIO_001121
.
}
dgn-np:NP618868.RADr4kCQMMt_uDmlFSwaT4XsKS3lg_dEDl2lNCX10LDyk130_provenance
{
dgn-np:NP618868.RADr4kCQMMt_uDmlFSwaT4XsKS3lg_dEDl2lNCX10LDyk130_assertion
dcterms:description
"[Distinguishing effects of individual loci in the major histocompatibility complex (MHC) region are difficult due to the complex linkage disequilibrium (LD) pattern characterized by high LD, punctuated by recombination hot spots.]. 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:18650831
;
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:NP618868.RADr4kCQMMt_uDmlFSwaT4XsKS3lg_dEDl2lNCX10LDyk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:14+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" .
}