@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP618952.RA99Q92xWsufzKBGAtIzTsEFoK75AKt5d0QAJ96QTXseY
> .
@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:NP618952.RA99Q92xWsufzKBGAtIzTsEFoK75AKt5d0QAJ96QTXseY130_head
{
this:
np:hasAssertion
dgn-np:NP618952.RA99Q92xWsufzKBGAtIzTsEFoK75AKt5d0QAJ96QTXseY130_assertion
;
np:hasProvenance
dgn-np:NP618952.RA99Q92xWsufzKBGAtIzTsEFoK75AKt5d0QAJ96QTXseY130_provenance
;
np:hasPublicationInfo
dgn-np:NP618952.RA99Q92xWsufzKBGAtIzTsEFoK75AKt5d0QAJ96QTXseY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP618952.RA99Q92xWsufzKBGAtIzTsEFoK75AKt5d0QAJ96QTXseY130_assertion
a
np:Assertion
.
dgn-np:NP618952.RA99Q92xWsufzKBGAtIzTsEFoK75AKt5d0QAJ96QTXseY130_provenance
a
np:Provenance
.
dgn-np:NP618952.RA99Q92xWsufzKBGAtIzTsEFoK75AKt5d0QAJ96QTXseY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP618952.RA99Q92xWsufzKBGAtIzTsEFoK75AKt5d0QAJ96QTXseY130_assertion
{
miriam-gene:25797
a
ncit:C16612
.
lld:C0205851
a
ncit:C7057
.
dgn-gda:DGNef9653879311a47e940125b016460598
sio:SIO_000628
miriam-gene:25797
,
lld:C0205851
;
a
sio:SIO_001121
.
}
dgn-np:NP618952.RA99Q92xWsufzKBGAtIzTsEFoK75AKt5d0QAJ96QTXseY130_provenance
{
dgn-np:NP618952.RA99Q92xWsufzKBGAtIzTsEFoK75AKt5d0QAJ96QTXseY130_assertion
dcterms:description
"[We further localized the gene between the polymorphic markers D12S1671 and D12S1082 at 12q22 to determine the role of APAF1 in the pathogenesis of GCT, and we characterized its normal genomic structure and analyzed its alterations in GCTs.]. 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:10862031
;
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:NP618952.RA99Q92xWsufzKBGAtIzTsEFoK75AKt5d0QAJ96QTXseY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:14+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" .
}