@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP200665.RA7FNHNS_FfsGBXsvTu6JmpS4h4OcIJXd2zA6cJtpnD1c
> .
@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:NP200665.RA7FNHNS_FfsGBXsvTu6JmpS4h4OcIJXd2zA6cJtpnD1c130_head
{
this:
np:hasAssertion
dgn-np:NP200665.RA7FNHNS_FfsGBXsvTu6JmpS4h4OcIJXd2zA6cJtpnD1c130_assertion
;
np:hasProvenance
dgn-np:NP200665.RA7FNHNS_FfsGBXsvTu6JmpS4h4OcIJXd2zA6cJtpnD1c130_provenance
;
np:hasPublicationInfo
dgn-np:NP200665.RA7FNHNS_FfsGBXsvTu6JmpS4h4OcIJXd2zA6cJtpnD1c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP200665.RA7FNHNS_FfsGBXsvTu6JmpS4h4OcIJXd2zA6cJtpnD1c130_assertion
a
np:Assertion
.
dgn-np:NP200665.RA7FNHNS_FfsGBXsvTu6JmpS4h4OcIJXd2zA6cJtpnD1c130_provenance
a
np:Provenance
.
dgn-np:NP200665.RA7FNHNS_FfsGBXsvTu6JmpS4h4OcIJXd2zA6cJtpnD1c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP200665.RA7FNHNS_FfsGBXsvTu6JmpS4h4OcIJXd2zA6cJtpnD1c130_assertion
{
miriam-gene:8091
a
ncit:C16612
.
lld:C1306242
a
ncit:C7057
.
dgn-gda:DGNe65466f0782c3c34ac5a11db3b419b21
sio:SIO_000628
miriam-gene:8091
,
lld:C1306242
;
a
sio:SIO_001121
.
}
dgn-np:NP200665.RA7FNHNS_FfsGBXsvTu6JmpS4h4OcIJXd2zA6cJtpnD1c130_provenance
{
dgn-np:NP200665.RA7FNHNS_FfsGBXsvTu6JmpS4h4OcIJXd2zA6cJtpnD1c130_assertion
dcterms:description
"[Starting from the ectopic sequence derived from an HMGIC fusion transcript of an aggressive angiomyxoma with such an inversion we established three PAC clones covering the breakpoint region 12p11 and cloned part of a yet unknown gene in 12p11.2, which is fused to the third exon of HMGIC.]. 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:9466569
;
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:NP200665.RA7FNHNS_FfsGBXsvTu6JmpS4h4OcIJXd2zA6cJtpnD1c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:50+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" .
}