@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP292394.RAyao9sayX3_SQrJeDWN2c9MGvpxhmKk-0QbycQdB2_uQ
> .
@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:NP292394.RAyao9sayX3_SQrJeDWN2c9MGvpxhmKk-0QbycQdB2_uQ130_head
{
this:
np:hasAssertion
dgn-np:NP292394.RAyao9sayX3_SQrJeDWN2c9MGvpxhmKk-0QbycQdB2_uQ130_assertion
;
np:hasProvenance
dgn-np:NP292394.RAyao9sayX3_SQrJeDWN2c9MGvpxhmKk-0QbycQdB2_uQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP292394.RAyao9sayX3_SQrJeDWN2c9MGvpxhmKk-0QbycQdB2_uQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP292394.RAyao9sayX3_SQrJeDWN2c9MGvpxhmKk-0QbycQdB2_uQ130_assertion
a
np:Assertion
.
dgn-np:NP292394.RAyao9sayX3_SQrJeDWN2c9MGvpxhmKk-0QbycQdB2_uQ130_provenance
a
np:Provenance
.
dgn-np:NP292394.RAyao9sayX3_SQrJeDWN2c9MGvpxhmKk-0QbycQdB2_uQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP292394.RAyao9sayX3_SQrJeDWN2c9MGvpxhmKk-0QbycQdB2_uQ130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0205851
a
ncit:C7057
.
dgn-gda:DGN925a487462a23bdc37d86f82ec3a2ae5
sio:SIO_000628
miriam-gene:7157
,
lld:C0205851
;
a
sio:SIO_001121
.
}
dgn-np:NP292394.RAyao9sayX3_SQrJeDWN2c9MGvpxhmKk-0QbycQdB2_uQ130_provenance
{
dgn-np:NP292394.RAyao9sayX3_SQrJeDWN2c9MGvpxhmKk-0QbycQdB2_uQ130_assertion
dcterms:description
"[No losses were found on 12q and 17p despite the fact that the most common cytogenetic abnormality in TGCTs is an i(12p) and that the TP53 gene on 17p is the most frequently mutated gene in human cancers.]. 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:7547632
;
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:NP292394.RAyao9sayX3_SQrJeDWN2c9MGvpxhmKk-0QbycQdB2_uQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:46+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" .
}