@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP916396.RAff5Qdkz2G6fZog0skwzLMKxxLtItyN5ubgtNg0Sl8DY
> .
@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:NP916396.RAff5Qdkz2G6fZog0skwzLMKxxLtItyN5ubgtNg0Sl8DY130_head
{
this:
np:hasAssertion
dgn-np:NP916396.RAff5Qdkz2G6fZog0skwzLMKxxLtItyN5ubgtNg0Sl8DY130_assertion
;
np:hasProvenance
dgn-np:NP916396.RAff5Qdkz2G6fZog0skwzLMKxxLtItyN5ubgtNg0Sl8DY130_provenance
;
np:hasPublicationInfo
dgn-np:NP916396.RAff5Qdkz2G6fZog0skwzLMKxxLtItyN5ubgtNg0Sl8DY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP916396.RAff5Qdkz2G6fZog0skwzLMKxxLtItyN5ubgtNg0Sl8DY130_assertion
a
np:Assertion
.
dgn-np:NP916396.RAff5Qdkz2G6fZog0skwzLMKxxLtItyN5ubgtNg0Sl8DY130_provenance
a
np:Provenance
.
dgn-np:NP916396.RAff5Qdkz2G6fZog0skwzLMKxxLtItyN5ubgtNg0Sl8DY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP916396.RAff5Qdkz2G6fZog0skwzLMKxxLtItyN5ubgtNg0Sl8DY130_assertion
{
miriam-gene:5155
a
ncit:C16612
.
lld:C0027533
a
ncit:C7057
.
dgn-gda:DGN99c616077b35b99e926bc4c50aa4448e
sio:SIO_000628
miriam-gene:5155
,
lld:C0027533
;
a
sio:SIO_001121
.
}
dgn-np:NP916396.RAff5Qdkz2G6fZog0skwzLMKxxLtItyN5ubgtNg0Sl8DY130_provenance
{
dgn-np:NP916396.RAff5Qdkz2G6fZog0skwzLMKxxLtItyN5ubgtNg0Sl8DY130_assertion
dcterms:description
"[The target genes ECGFB, DIA1, BIK, and PDGFB and the microsatellite markers D22S274 and D22S277, mapped on 22q13, were selected according to our previous loss of heterozygosity findings in head and neck tumors.]. 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:12226751
;
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:NP916396.RAff5Qdkz2G6fZog0skwzLMKxxLtItyN5ubgtNg0Sl8DY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:22+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" .
}