@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP194364.RAKtDhbnw2f2sfWUaVT5mYnjSe8RJhDef81PeClrmpRT8
> .
@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:NP194364.RAKtDhbnw2f2sfWUaVT5mYnjSe8RJhDef81PeClrmpRT8130_head
{
this:
np:hasAssertion
dgn-np:NP194364.RAKtDhbnw2f2sfWUaVT5mYnjSe8RJhDef81PeClrmpRT8130_assertion
;
np:hasProvenance
dgn-np:NP194364.RAKtDhbnw2f2sfWUaVT5mYnjSe8RJhDef81PeClrmpRT8130_provenance
;
np:hasPublicationInfo
dgn-np:NP194364.RAKtDhbnw2f2sfWUaVT5mYnjSe8RJhDef81PeClrmpRT8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP194364.RAKtDhbnw2f2sfWUaVT5mYnjSe8RJhDef81PeClrmpRT8130_assertion
a
np:Assertion
.
dgn-np:NP194364.RAKtDhbnw2f2sfWUaVT5mYnjSe8RJhDef81PeClrmpRT8130_provenance
a
np:Provenance
.
dgn-np:NP194364.RAKtDhbnw2f2sfWUaVT5mYnjSe8RJhDef81PeClrmpRT8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP194364.RAKtDhbnw2f2sfWUaVT5mYnjSe8RJhDef81PeClrmpRT8130_assertion
{
miriam-gene:677775
a
ncit:C16612
.
lld:C0017638
a
ncit:C7057
.
dgn-gda:DGNde9720fac73adc955d312e6b5a970619
sio:SIO_000628
miriam-gene:677775
,
lld:C0017638
;
a
sio:SIO_001121
.
}
dgn-np:NP194364.RAKtDhbnw2f2sfWUaVT5mYnjSe8RJhDef81PeClrmpRT8130_provenance
{
dgn-np:NP194364.RAKtDhbnw2f2sfWUaVT5mYnjSe8RJhDef81PeClrmpRT8130_assertion
dcterms:description
"[Cell lines A172 and U87 contain 1p and 19q deletions similar to those found in sporadic gliomas and will be useful cellular reagents for evaluating the function of putative 1p and 19q glioma tumor suppressor genes.]. 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:15949564
;
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:NP194364.RAKtDhbnw2f2sfWUaVT5mYnjSe8RJhDef81PeClrmpRT8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:47+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" .
}