@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP50158.RAl4Xlmzp03Js4qNpDDrVolDMWfOhEmeSkHzNDsnI2kv0
> .
@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:NP50158.RAl4Xlmzp03Js4qNpDDrVolDMWfOhEmeSkHzNDsnI2kv0130_head
{
this:
np:hasAssertion
dgn-np:NP50158.RAl4Xlmzp03Js4qNpDDrVolDMWfOhEmeSkHzNDsnI2kv0130_assertion
;
np:hasProvenance
dgn-np:NP50158.RAl4Xlmzp03Js4qNpDDrVolDMWfOhEmeSkHzNDsnI2kv0130_provenance
;
np:hasPublicationInfo
dgn-np:NP50158.RAl4Xlmzp03Js4qNpDDrVolDMWfOhEmeSkHzNDsnI2kv0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP50158.RAl4Xlmzp03Js4qNpDDrVolDMWfOhEmeSkHzNDsnI2kv0130_assertion
a
np:Assertion
.
dgn-np:NP50158.RAl4Xlmzp03Js4qNpDDrVolDMWfOhEmeSkHzNDsnI2kv0130_provenance
a
np:Provenance
.
dgn-np:NP50158.RAl4Xlmzp03Js4qNpDDrVolDMWfOhEmeSkHzNDsnI2kv0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP50158.RAl4Xlmzp03Js4qNpDDrVolDMWfOhEmeSkHzNDsnI2kv0130_assertion
{
miriam-gene:7124
a
ncit:C16612
.
lld:C0009324
a
ncit:C7057
.
dgn-gda:DGN1576af0c16d08e8e9a47ffa37295bb57
sio:SIO_000628
miriam-gene:7124
,
lld:C0009324
;
a
sio:SIO_001122
.
}
dgn-np:NP50158.RAl4Xlmzp03Js4qNpDDrVolDMWfOhEmeSkHzNDsnI2kv0130_provenance
{
dgn-np:NP50158.RAl4Xlmzp03Js4qNpDDrVolDMWfOhEmeSkHzNDsnI2kv0130_assertion
dcterms:description
"[ The above-mentioned pattern, most likely formed by recombination of the telomeric fragment of the MHC 7.1 ancestral haplotype, seems to be the most important genetic determinant of susceptibility to the extensive form of UC in our population.]. 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:16116311
;
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:NP50158.RAl4Xlmzp03Js4qNpDDrVolDMWfOhEmeSkHzNDsnI2kv0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:23+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" .
}