@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP50818.RAx6wZmxT961DHtGtQtgqsBHoVgjpEkyOMGF4N9hSQRwA
> .
@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:NP50818.RAx6wZmxT961DHtGtQtgqsBHoVgjpEkyOMGF4N9hSQRwA130_head
{
this:
np:hasAssertion
dgn-np:NP50818.RAx6wZmxT961DHtGtQtgqsBHoVgjpEkyOMGF4N9hSQRwA130_assertion
;
np:hasProvenance
dgn-np:NP50818.RAx6wZmxT961DHtGtQtgqsBHoVgjpEkyOMGF4N9hSQRwA130_provenance
;
np:hasPublicationInfo
dgn-np:NP50818.RAx6wZmxT961DHtGtQtgqsBHoVgjpEkyOMGF4N9hSQRwA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP50818.RAx6wZmxT961DHtGtQtgqsBHoVgjpEkyOMGF4N9hSQRwA130_assertion
a
np:Assertion
.
dgn-np:NP50818.RAx6wZmxT961DHtGtQtgqsBHoVgjpEkyOMGF4N9hSQRwA130_provenance
a
np:Provenance
.
dgn-np:NP50818.RAx6wZmxT961DHtGtQtgqsBHoVgjpEkyOMGF4N9hSQRwA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP50818.RAx6wZmxT961DHtGtQtgqsBHoVgjpEkyOMGF4N9hSQRwA130_assertion
{
miriam-gene:30009
a
ncit:C16612
.
lld:C0004096
a
ncit:C7057
.
dgn-gda:DGN991e4648f2a2a8aaa2f49ee291465b2d
sio:SIO_000628
miriam-gene:30009
,
lld:C0004096
;
a
sio:SIO_001122
.
}
dgn-np:NP50818.RAx6wZmxT961DHtGtQtgqsBHoVgjpEkyOMGF4N9hSQRwA130_provenance
{
dgn-np:NP50818.RAx6wZmxT961DHtGtQtgqsBHoVgjpEkyOMGF4N9hSQRwA130_assertion
dcterms:description
"[In order to examine whether polymorphisms in the candidate gene, TBX21, located on chromosome 17q21.32, are related to the risk of human asthma phenotypes, we have searched for genetic variations in the human TBX21 gene and identified 24 single nucleotide polymorphisms (SNPs), including five novel SNPs, by direct sequencing in Japanese subjects.]. 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:15806396
;
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:NP50818.RAx6wZmxT961DHtGtQtgqsBHoVgjpEkyOMGF4N9hSQRwA130_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" .
}