@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP881323.RACG1Dnr226MD2MM4vOojtuWwlDVg5jMUnudOOmAPoW7I
> .
@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:NP881323.RACG1Dnr226MD2MM4vOojtuWwlDVg5jMUnudOOmAPoW7I130_head
{
this:
np:hasAssertion
dgn-np:NP881323.RACG1Dnr226MD2MM4vOojtuWwlDVg5jMUnudOOmAPoW7I130_assertion
;
np:hasProvenance
dgn-np:NP881323.RACG1Dnr226MD2MM4vOojtuWwlDVg5jMUnudOOmAPoW7I130_provenance
;
np:hasPublicationInfo
dgn-np:NP881323.RACG1Dnr226MD2MM4vOojtuWwlDVg5jMUnudOOmAPoW7I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP881323.RACG1Dnr226MD2MM4vOojtuWwlDVg5jMUnudOOmAPoW7I130_assertion
a
np:Assertion
.
dgn-np:NP881323.RACG1Dnr226MD2MM4vOojtuWwlDVg5jMUnudOOmAPoW7I130_provenance
a
np:Provenance
.
dgn-np:NP881323.RACG1Dnr226MD2MM4vOojtuWwlDVg5jMUnudOOmAPoW7I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP881323.RACG1Dnr226MD2MM4vOojtuWwlDVg5jMUnudOOmAPoW7I130_assertion
{
miriam-gene:1030
a
ncit:C16612
.
lld:C0004114
a
ncit:C7057
.
dgn-gda:DGNa316dbaebb2a9501f6c4b400c7bd20b6
sio:SIO_000628
miriam-gene:1030
,
lld:C0004114
;
a
sio:SIO_001121
.
}
dgn-np:NP881323.RACG1Dnr226MD2MM4vOojtuWwlDVg5jMUnudOOmAPoW7I130_provenance
{
dgn-np:NP881323.RACG1Dnr226MD2MM4vOojtuWwlDVg5jMUnudOOmAPoW7I130_assertion
dcterms:description
"[In a series of 46 glioblastomas, 16 anaplastic astrocytomas and eight astrocytomas, all tumours retaining one or both alleles of CDKN2A (48 tumours) and CDKN2B (49 tumours) were subjected to sequence analysis (entire coding region and splice acceptor and donor sites).]. 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:9000591
;
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:NP881323.RACG1Dnr226MD2MM4vOojtuWwlDVg5jMUnudOOmAPoW7I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:58+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" .
}