@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1412723.RAGHikp528wXdlGfQr1RbKtaQZgfM6OAcK9DJQNqajV68
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1412723.RAGHikp528wXdlGfQr1RbKtaQZgfM6OAcK9DJQNqajV68130_head
{
this:
np:hasAssertion
dgn-np:NP1412723.RAGHikp528wXdlGfQr1RbKtaQZgfM6OAcK9DJQNqajV68130_assertion
;
np:hasProvenance
dgn-np:NP1412723.RAGHikp528wXdlGfQr1RbKtaQZgfM6OAcK9DJQNqajV68130_provenance
;
np:hasPublicationInfo
dgn-np:NP1412723.RAGHikp528wXdlGfQr1RbKtaQZgfM6OAcK9DJQNqajV68130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1412723.RAGHikp528wXdlGfQr1RbKtaQZgfM6OAcK9DJQNqajV68130_assertion
a
np:Assertion
.
dgn-np:NP1412723.RAGHikp528wXdlGfQr1RbKtaQZgfM6OAcK9DJQNqajV68130_provenance
a
np:Provenance
.
dgn-np:NP1412723.RAGHikp528wXdlGfQr1RbKtaQZgfM6OAcK9DJQNqajV68130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1412723.RAGHikp528wXdlGfQr1RbKtaQZgfM6OAcK9DJQNqajV68130_assertion
{
miriam-gene:7750
a
ncit:C16612
.
lld:C2827362
a
ncit:C7057
.
dgn-gda:DGN1a9fcd432eb90b84f44c2d8ab4551b17
sio:SIO_000628
miriam-gene:7750
,
lld:C2827362
;
a
sio:SIO_001122
.
}
dgn-np:NP1412723.RAGHikp528wXdlGfQr1RbKtaQZgfM6OAcK9DJQNqajV68130_provenance
{
dgn-np:NP1412723.RAGHikp528wXdlGfQr1RbKtaQZgfM6OAcK9DJQNqajV68130_assertion
dcterms:description
"[The t(8;13)(p11;q12) is the most common translocation associated with the 8p11 myeloproliferative syndrome and results in an identical mRNA fusion between ZNF198 at 13q12 and FGFR1 at 8p11 in all cases thus far reported.]. 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:9889006
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1412723.RAGHikp528wXdlGfQr1RbKtaQZgfM6OAcK9DJQNqajV68130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:27+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}