@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP624961.RAytazkIIdD-7srv2cnZMtT_P81ZtMxNFZyhS3iZkzNPg
> .
@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:NP624961.RAytazkIIdD-7srv2cnZMtT_P81ZtMxNFZyhS3iZkzNPg130_head
{
this:
np:hasAssertion
dgn-np:NP624961.RAytazkIIdD-7srv2cnZMtT_P81ZtMxNFZyhS3iZkzNPg130_assertion
;
np:hasProvenance
dgn-np:NP624961.RAytazkIIdD-7srv2cnZMtT_P81ZtMxNFZyhS3iZkzNPg130_provenance
;
np:hasPublicationInfo
dgn-np:NP624961.RAytazkIIdD-7srv2cnZMtT_P81ZtMxNFZyhS3iZkzNPg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP624961.RAytazkIIdD-7srv2cnZMtT_P81ZtMxNFZyhS3iZkzNPg130_assertion
a
np:Assertion
.
dgn-np:NP624961.RAytazkIIdD-7srv2cnZMtT_P81ZtMxNFZyhS3iZkzNPg130_provenance
a
np:Provenance
.
dgn-np:NP624961.RAytazkIIdD-7srv2cnZMtT_P81ZtMxNFZyhS3iZkzNPg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP624961.RAytazkIIdD-7srv2cnZMtT_P81ZtMxNFZyhS3iZkzNPg130_assertion
{
miriam-gene:2669
a
ncit:C16612
.
lld:C0086525
a
ncit:C7057
.
dgn-gda:DGN1cc51712fcb37196aad51643e3813874
sio:SIO_000628
miriam-gene:2669
,
lld:C0086525
;
a
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.
}
dgn-np:NP624961.RAytazkIIdD-7srv2cnZMtT_P81ZtMxNFZyhS3iZkzNPg130_provenance
{
dgn-np:NP624961.RAytazkIIdD-7srv2cnZMtT_P81ZtMxNFZyhS3iZkzNPg130_assertion
dcterms:description
"[A comparison of several statistical methods and measures (gene frequency, haplotype frequency, and linkage disequilibrium estimation) using the Centre d'Etude du Polymorphisme Humain data will be provided using KIR haplotypes that have been determined by segregation analysis, noting the strengths and weaknesses of the methods when only the presence/absence data is considered.]. 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:18797862
;
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:NP624961.RAytazkIIdD-7srv2cnZMtT_P81ZtMxNFZyhS3iZkzNPg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:17+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" .
}