@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP235272.RA7Rm-ii3cMZARF5iaPfgrj1C-bIF3wlIZIvfuoa1qjaw
> .
@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:NP235272.RA7Rm-ii3cMZARF5iaPfgrj1C-bIF3wlIZIvfuoa1qjaw130_head
{
this:
np:hasAssertion
dgn-np:NP235272.RA7Rm-ii3cMZARF5iaPfgrj1C-bIF3wlIZIvfuoa1qjaw130_assertion
;
np:hasProvenance
dgn-np:NP235272.RA7Rm-ii3cMZARF5iaPfgrj1C-bIF3wlIZIvfuoa1qjaw130_provenance
;
np:hasPublicationInfo
dgn-np:NP235272.RA7Rm-ii3cMZARF5iaPfgrj1C-bIF3wlIZIvfuoa1qjaw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP235272.RA7Rm-ii3cMZARF5iaPfgrj1C-bIF3wlIZIvfuoa1qjaw130_assertion
a
np:Assertion
.
dgn-np:NP235272.RA7Rm-ii3cMZARF5iaPfgrj1C-bIF3wlIZIvfuoa1qjaw130_provenance
a
np:Provenance
.
dgn-np:NP235272.RA7Rm-ii3cMZARF5iaPfgrj1C-bIF3wlIZIvfuoa1qjaw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP235272.RA7Rm-ii3cMZARF5iaPfgrj1C-bIF3wlIZIvfuoa1qjaw130_assertion
{
miriam-gene:2967
a
ncit:C16612
.
lld:C0266573
a
ncit:C7057
.
dgn-gda:DGN7375a358de5cefccb6f8cafde1a0f6c2
sio:SIO_000628
miriam-gene:2967
,
lld:C0266573
;
a
sio:SIO_001121
.
}
dgn-np:NP235272.RA7Rm-ii3cMZARF5iaPfgrj1C-bIF3wlIZIvfuoa1qjaw130_provenance
{
dgn-np:NP235272.RA7Rm-ii3cMZARF5iaPfgrj1C-bIF3wlIZIvfuoa1qjaw130_assertion
dcterms:description
"[In addition, in a sporadic case with a balanced chromosomal translocation t(1;8) (p34.3;q21.12), the ZFHX4 (zinc finger homeodomain 4) gene was found to be disrupted at the 8q21.12 breakpoint, but there was no gene at the 1p34.3 breakpoint, suggesting the existence of the third PTOS locus (PTOS1) at 8q21.12.]. 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:17987257
;
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:NP235272.RA7Rm-ii3cMZARF5iaPfgrj1C-bIF3wlIZIvfuoa1qjaw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:12+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" .
}