@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP58185.RAtlPqHjlZq8Bhb0H6cmS1ZAgh_zh9moROKbOeH3KphCU
> .
@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:NP58185.RAtlPqHjlZq8Bhb0H6cmS1ZAgh_zh9moROKbOeH3KphCU130_head
{
this:
np:hasAssertion
dgn-np:NP58185.RAtlPqHjlZq8Bhb0H6cmS1ZAgh_zh9moROKbOeH3KphCU130_assertion
;
np:hasProvenance
dgn-np:NP58185.RAtlPqHjlZq8Bhb0H6cmS1ZAgh_zh9moROKbOeH3KphCU130_provenance
;
np:hasPublicationInfo
dgn-np:NP58185.RAtlPqHjlZq8Bhb0H6cmS1ZAgh_zh9moROKbOeH3KphCU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP58185.RAtlPqHjlZq8Bhb0H6cmS1ZAgh_zh9moROKbOeH3KphCU130_assertion
a
np:Assertion
.
dgn-np:NP58185.RAtlPqHjlZq8Bhb0H6cmS1ZAgh_zh9moROKbOeH3KphCU130_provenance
a
np:Provenance
.
dgn-np:NP58185.RAtlPqHjlZq8Bhb0H6cmS1ZAgh_zh9moROKbOeH3KphCU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP58185.RAtlPqHjlZq8Bhb0H6cmS1ZAgh_zh9moROKbOeH3KphCU130_assertion
{
miriam-gene:3115
a
ncit:C16612
.
lld:C0024299
a
ncit:C7057
.
dgn-gda:DGN6f5cf73f3cc6562b1811f8961b99eaee
sio:SIO_000628
miriam-gene:3115
,
lld:C0024299
;
a
sio:SIO_001122
.
}
dgn-np:NP58185.RAtlPqHjlZq8Bhb0H6cmS1ZAgh_zh9moROKbOeH3KphCU130_provenance
{
dgn-np:NP58185.RAtlPqHjlZq8Bhb0H6cmS1ZAgh_zh9moROKbOeH3KphCU130_assertion
dcterms:description
"[These data can be used as control data for HLA disease associations and paternity studies, but they are also important for the evaluation of the probability rate of success in determining the optimal matched donor in unrelated stem transplantation for Tunisian patients or patients of Tunisian origin.]. 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:15361135
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP58185.RAtlPqHjlZq8Bhb0H6cmS1ZAgh_zh9moROKbOeH3KphCU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:27+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" .
}