@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP43856.RAHQpBwZExJW5l4WxMcB3mOsYqTIc2ZiprXybP71bps_c
> .
@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:NP43856.RAHQpBwZExJW5l4WxMcB3mOsYqTIc2ZiprXybP71bps_c130_head
{
this:
np:hasAssertion
dgn-np:NP43856.RAHQpBwZExJW5l4WxMcB3mOsYqTIc2ZiprXybP71bps_c130_assertion
;
np:hasProvenance
dgn-np:NP43856.RAHQpBwZExJW5l4WxMcB3mOsYqTIc2ZiprXybP71bps_c130_provenance
;
np:hasPublicationInfo
dgn-np:NP43856.RAHQpBwZExJW5l4WxMcB3mOsYqTIc2ZiprXybP71bps_c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP43856.RAHQpBwZExJW5l4WxMcB3mOsYqTIc2ZiprXybP71bps_c130_assertion
a
np:Assertion
.
dgn-np:NP43856.RAHQpBwZExJW5l4WxMcB3mOsYqTIc2ZiprXybP71bps_c130_provenance
a
np:Provenance
.
dgn-np:NP43856.RAHQpBwZExJW5l4WxMcB3mOsYqTIc2ZiprXybP71bps_c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP43856.RAHQpBwZExJW5l4WxMcB3mOsYqTIc2ZiprXybP71bps_c130_assertion
{
miriam-gene:2524
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGNe07376dacae4395e73e2c73a1481c4fc
sio:SIO_000628
miriam-gene:2524
,
lld:C0030567
;
a
sio:SIO_001122
.
}
dgn-np:NP43856.RAHQpBwZExJW5l4WxMcB3mOsYqTIc2ZiprXybP71bps_c130_provenance
{
dgn-np:NP43856.RAHQpBwZExJW5l4WxMcB3mOsYqTIc2ZiprXybP71bps_c130_assertion
dcterms:description
"[The fusion gene was not found in the two investigated ethnic groups. The frequencies of G849A nonsense mutation in Shandong Han Chinese and Mongolian of Inner Mongolia individuals were the same, 0.0055.]. 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:12645255
;
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:NP43856.RAHQpBwZExJW5l4WxMcB3mOsYqTIc2ZiprXybP71bps_c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:20+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" .
}