@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP855507.RApvRRsad-jMuHTKOXGHpqOjPqGxERIJtd3icxk-crcVo
> .
@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:NP855507.RApvRRsad-jMuHTKOXGHpqOjPqGxERIJtd3icxk-crcVo130_head
{
this:
np:hasAssertion
dgn-np:NP855507.RApvRRsad-jMuHTKOXGHpqOjPqGxERIJtd3icxk-crcVo130_assertion
;
np:hasProvenance
dgn-np:NP855507.RApvRRsad-jMuHTKOXGHpqOjPqGxERIJtd3icxk-crcVo130_provenance
;
np:hasPublicationInfo
dgn-np:NP855507.RApvRRsad-jMuHTKOXGHpqOjPqGxERIJtd3icxk-crcVo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP855507.RApvRRsad-jMuHTKOXGHpqOjPqGxERIJtd3icxk-crcVo130_assertion
a
np:Assertion
.
dgn-np:NP855507.RApvRRsad-jMuHTKOXGHpqOjPqGxERIJtd3icxk-crcVo130_provenance
a
np:Provenance
.
dgn-np:NP855507.RApvRRsad-jMuHTKOXGHpqOjPqGxERIJtd3icxk-crcVo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP855507.RApvRRsad-jMuHTKOXGHpqOjPqGxERIJtd3icxk-crcVo130_assertion
{
miriam-gene:619501
a
ncit:C16612
.
lld:C0260037
a
ncit:C7057
.
dgn-gda:DGN30515e56c9917d0f0db3749c1fb5b7dc
sio:SIO_000628
miriam-gene:619501
,
lld:C0260037
;
a
sio:SIO_001121
.
}
dgn-np:NP855507.RApvRRsad-jMuHTKOXGHpqOjPqGxERIJtd3icxk-crcVo130_provenance
{
dgn-np:NP855507.RApvRRsad-jMuHTKOXGHpqOjPqGxERIJtd3icxk-crcVo130_assertion
dcterms:description
"[In order to clarify the origin of multiple tumors of HCC genetically, we examined patterns of loss of heterozygosity (LOH) on chromosome 16 for DNA isolated from 43 HCCs resected from 19 patients by analysis of restriction fragment length polymorphism.]. 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:1347253
;
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:NP855507.RApvRRsad-jMuHTKOXGHpqOjPqGxERIJtd3icxk-crcVo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:43+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" .
}