@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP538630.RAYJ8MKr_oiWZ98qCM8vof8XuCX0rV6_Us8pE7hfu7Kqw
> .
@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:NP538630.RAYJ8MKr_oiWZ98qCM8vof8XuCX0rV6_Us8pE7hfu7Kqw130_head
{
this:
np:hasAssertion
dgn-np:NP538630.RAYJ8MKr_oiWZ98qCM8vof8XuCX0rV6_Us8pE7hfu7Kqw130_assertion
;
np:hasProvenance
dgn-np:NP538630.RAYJ8MKr_oiWZ98qCM8vof8XuCX0rV6_Us8pE7hfu7Kqw130_provenance
;
np:hasPublicationInfo
dgn-np:NP538630.RAYJ8MKr_oiWZ98qCM8vof8XuCX0rV6_Us8pE7hfu7Kqw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP538630.RAYJ8MKr_oiWZ98qCM8vof8XuCX0rV6_Us8pE7hfu7Kqw130_assertion
a
np:Assertion
.
dgn-np:NP538630.RAYJ8MKr_oiWZ98qCM8vof8XuCX0rV6_Us8pE7hfu7Kqw130_provenance
a
np:Provenance
.
dgn-np:NP538630.RAYJ8MKr_oiWZ98qCM8vof8XuCX0rV6_Us8pE7hfu7Kqw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP538630.RAYJ8MKr_oiWZ98qCM8vof8XuCX0rV6_Us8pE7hfu7Kqw130_assertion
{
miriam-gene:4771
a
ncit:C16612
.
lld:C1847319
a
ncit:C7057
.
dgn-gda:DGN07c0ace9d047ef32941486449c8049a1
sio:SIO_000628
miriam-gene:4771
,
lld:C1847319
;
a
sio:SIO_001121
.
}
dgn-np:NP538630.RAYJ8MKr_oiWZ98qCM8vof8XuCX0rV6_Us8pE7hfu7Kqw130_provenance
{
dgn-np:NP538630.RAYJ8MKr_oiWZ98qCM8vof8XuCX0rV6_Us8pE7hfu7Kqw130_assertion
dcterms:description
"[The findings suggest that allelic losses at 22q are associated with high mitotic activity and recurring disease, and that alterations in the NF2 gene are unlikely to participate in the pathogenesis of GIST.]. 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:14562282
;
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:NP538630.RAYJ8MKr_oiWZ98qCM8vof8XuCX0rV6_Us8pE7hfu7Kqw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:25+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" .
}