@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP462666.RA_2QPorc8qynH3Kkt82QE9l6iDgOv41XM4JnixaMwBZk
> .
@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:NP462666.RA_2QPorc8qynH3Kkt82QE9l6iDgOv41XM4JnixaMwBZk130_head
{
this:
np:hasAssertion
dgn-np:NP462666.RA_2QPorc8qynH3Kkt82QE9l6iDgOv41XM4JnixaMwBZk130_assertion
;
np:hasProvenance
dgn-np:NP462666.RA_2QPorc8qynH3Kkt82QE9l6iDgOv41XM4JnixaMwBZk130_provenance
;
np:hasPublicationInfo
dgn-np:NP462666.RA_2QPorc8qynH3Kkt82QE9l6iDgOv41XM4JnixaMwBZk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP462666.RA_2QPorc8qynH3Kkt82QE9l6iDgOv41XM4JnixaMwBZk130_assertion
a
np:Assertion
.
dgn-np:NP462666.RA_2QPorc8qynH3Kkt82QE9l6iDgOv41XM4JnixaMwBZk130_provenance
a
np:Provenance
.
dgn-np:NP462666.RA_2QPorc8qynH3Kkt82QE9l6iDgOv41XM4JnixaMwBZk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP462666.RA_2QPorc8qynH3Kkt82QE9l6iDgOv41XM4JnixaMwBZk130_assertion
{
miriam-gene:29980
a
ncit:C16612
.
lld:C0011854
a
ncit:C7057
.
dgn-gda:DGN06f6f17217d4cbcb293378b4ffe8b8c8
sio:SIO_000628
miriam-gene:29980
,
lld:C0011854
;
a
sio:SIO_001121
.
}
dgn-np:NP462666.RA_2QPorc8qynH3Kkt82QE9l6iDgOv41XM4JnixaMwBZk130_provenance
{
dgn-np:NP462666.RA_2QPorc8qynH3Kkt82QE9l6iDgOv41XM4JnixaMwBZk130_assertion
dcterms:description
"[The second is an extended haplotype that has not been identified before (A2, Cw7, B17, 3F31, DR2, DQw1), and, due to the DR2 allele, we expected it to be decreased in IDDM.]. 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:1890017
;
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:NP462666.RA_2QPorc8qynH3Kkt82QE9l6iDgOv41XM4JnixaMwBZk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:35+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" .
}