@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP768192.RAPJutYNxOD1x6-zHeKqIFcQsv51Jkx20iFnKLHygdjnk
> .
@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:NP768192.RAPJutYNxOD1x6-zHeKqIFcQsv51Jkx20iFnKLHygdjnk130_head
{
this:
np:hasAssertion
dgn-np:NP768192.RAPJutYNxOD1x6-zHeKqIFcQsv51Jkx20iFnKLHygdjnk130_assertion
;
np:hasProvenance
dgn-np:NP768192.RAPJutYNxOD1x6-zHeKqIFcQsv51Jkx20iFnKLHygdjnk130_provenance
;
np:hasPublicationInfo
dgn-np:NP768192.RAPJutYNxOD1x6-zHeKqIFcQsv51Jkx20iFnKLHygdjnk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP768192.RAPJutYNxOD1x6-zHeKqIFcQsv51Jkx20iFnKLHygdjnk130_assertion
a
np:Assertion
.
dgn-np:NP768192.RAPJutYNxOD1x6-zHeKqIFcQsv51Jkx20iFnKLHygdjnk130_provenance
a
np:Provenance
.
dgn-np:NP768192.RAPJutYNxOD1x6-zHeKqIFcQsv51Jkx20iFnKLHygdjnk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP768192.RAPJutYNxOD1x6-zHeKqIFcQsv51Jkx20iFnKLHygdjnk130_assertion
{
miriam-gene:57498
a
ncit:C16612
.
lld:C0004096
a
ncit:C7057
.
dgn-gda:DGNd3d0fe5d59ce62af47e80c9ae5959952
sio:SIO_000628
miriam-gene:57498
,
lld:C0004096
;
a
sio:SIO_001121
.
}
dgn-np:NP768192.RAPJutYNxOD1x6-zHeKqIFcQsv51Jkx20iFnKLHygdjnk130_provenance
{
dgn-np:NP768192.RAPJutYNxOD1x6-zHeKqIFcQsv51Jkx20iFnKLHygdjnk130_assertion
dcterms:description
"[Using an allele refractory mutation screening (ARMS) test, blood (from 212 subjects, including asthmatic children, their parents and siblings) was tested for the presence of the normal and variant sequence of the IgE receptor FcepsilonRIbeta [homozygous normal sequence (Ile 181/Val 183, NN), the variant sequence (Leu 181/Leu 183, LL) and the heterozygous state NL].]. 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:11245344
;
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:NP768192.RAPJutYNxOD1x6-zHeKqIFcQsv51Jkx20iFnKLHygdjnk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:45+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" .
}