@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP808884.RAgMemq-5pPFqBNWqdmGTBBbtaOmbQK6B2d7Dv1Ve_2KI
> .
@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:NP808884.RAgMemq-5pPFqBNWqdmGTBBbtaOmbQK6B2d7Dv1Ve_2KI130_head
{
this:
np:hasAssertion
dgn-np:NP808884.RAgMemq-5pPFqBNWqdmGTBBbtaOmbQK6B2d7Dv1Ve_2KI130_assertion
;
np:hasProvenance
dgn-np:NP808884.RAgMemq-5pPFqBNWqdmGTBBbtaOmbQK6B2d7Dv1Ve_2KI130_provenance
;
np:hasPublicationInfo
dgn-np:NP808884.RAgMemq-5pPFqBNWqdmGTBBbtaOmbQK6B2d7Dv1Ve_2KI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP808884.RAgMemq-5pPFqBNWqdmGTBBbtaOmbQK6B2d7Dv1Ve_2KI130_assertion
a
np:Assertion
.
dgn-np:NP808884.RAgMemq-5pPFqBNWqdmGTBBbtaOmbQK6B2d7Dv1Ve_2KI130_provenance
a
np:Provenance
.
dgn-np:NP808884.RAgMemq-5pPFqBNWqdmGTBBbtaOmbQK6B2d7Dv1Ve_2KI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP808884.RAgMemq-5pPFqBNWqdmGTBBbtaOmbQK6B2d7Dv1Ve_2KI130_assertion
{
miriam-gene:472
a
ncit:C16612
.
lld:C1168401
a
ncit:C7057
.
dgn-gda:DGNa7da01bd8761fb16ac7528bc821d9a83
sio:SIO_000628
miriam-gene:472
,
lld:C1168401
;
a
sio:SIO_001121
.
}
dgn-np:NP808884.RAgMemq-5pPFqBNWqdmGTBBbtaOmbQK6B2d7Dv1Ve_2KI130_provenance
{
dgn-np:NP808884.RAgMemq-5pPFqBNWqdmGTBBbtaOmbQK6B2d7Dv1Ve_2KI130_assertion
dcterms:description
"[Characterization of HNSCC using fluorescence in situ hybridization (FISH) revealed concurrent partial loss of MRE11A, ATM, and H2AFX in all four cell lines with 11q13 amplification and in four of seven cell lines without 11q13 amplification.]. 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:17492757
;
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:NP808884.RAgMemq-5pPFqBNWqdmGTBBbtaOmbQK6B2d7Dv1Ve_2KI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:16+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" .
}