@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP60226.RAZe7dB_1TWQi1xVUxAvh026gRgqD8efx9id1YRy3uza4
> .
@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:NP60226.RAZe7dB_1TWQi1xVUxAvh026gRgqD8efx9id1YRy3uza4130_head
{
this:
np:hasAssertion
dgn-np:NP60226.RAZe7dB_1TWQi1xVUxAvh026gRgqD8efx9id1YRy3uza4130_assertion
;
np:hasProvenance
dgn-np:NP60226.RAZe7dB_1TWQi1xVUxAvh026gRgqD8efx9id1YRy3uza4130_provenance
;
np:hasPublicationInfo
dgn-np:NP60226.RAZe7dB_1TWQi1xVUxAvh026gRgqD8efx9id1YRy3uza4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP60226.RAZe7dB_1TWQi1xVUxAvh026gRgqD8efx9id1YRy3uza4130_assertion
a
np:Assertion
.
dgn-np:NP60226.RAZe7dB_1TWQi1xVUxAvh026gRgqD8efx9id1YRy3uza4130_provenance
a
np:Provenance
.
dgn-np:NP60226.RAZe7dB_1TWQi1xVUxAvh026gRgqD8efx9id1YRy3uza4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP60226.RAZe7dB_1TWQi1xVUxAvh026gRgqD8efx9id1YRy3uza4130_assertion
{
miriam-gene:2210
a
ncit:C16612
.
lld:C0004096
a
ncit:C7057
.
dgn-gda:DGN40ff857275fd74cfa9bc24c023db9653
sio:SIO_000628
miriam-gene:2210
,
lld:C0004096
;
a
sio:SIO_001122
.
}
dgn-np:NP60226.RAZe7dB_1TWQi1xVUxAvh026gRgqD8efx9id1YRy3uza4130_provenance
{
dgn-np:NP60226.RAZe7dB_1TWQi1xVUxAvh026gRgqD8efx9id1YRy3uza4130_assertion
dcterms:description
"[ These results suggest that E237G mutation of Fc epsilon RI-beta gene presents in people of Han nationality of southern China, and is correlated with asthma. There are the lack or very low frequencies of V183L and I181L mutations in people of Han nationality of southern China.]. 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:11802953
;
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:NP60226.RAZe7dB_1TWQi1xVUxAvh026gRgqD8efx9id1YRy3uza4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:28+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" .
}