@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP196013.RADbc5Ak9DVrYAIU5cICeQ8oO28vPUBEZzxv3cly2HnbA
> .
@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 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:NP196013.RADbc5Ak9DVrYAIU5cICeQ8oO28vPUBEZzxv3cly2HnbA130_head
{
this:
np:hasAssertion
dgn-np:NP196013.RADbc5Ak9DVrYAIU5cICeQ8oO28vPUBEZzxv3cly2HnbA130_assertion
;
np:hasProvenance
dgn-np:NP196013.RADbc5Ak9DVrYAIU5cICeQ8oO28vPUBEZzxv3cly2HnbA130_provenance
;
np:hasPublicationInfo
dgn-np:NP196013.RADbc5Ak9DVrYAIU5cICeQ8oO28vPUBEZzxv3cly2HnbA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP196013.RADbc5Ak9DVrYAIU5cICeQ8oO28vPUBEZzxv3cly2HnbA130_assertion
a
np:Assertion
.
dgn-np:NP196013.RADbc5Ak9DVrYAIU5cICeQ8oO28vPUBEZzxv3cly2HnbA130_provenance
a
np:Provenance
.
dgn-np:NP196013.RADbc5Ak9DVrYAIU5cICeQ8oO28vPUBEZzxv3cly2HnbA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP196013.RADbc5Ak9DVrYAIU5cICeQ8oO28vPUBEZzxv3cly2HnbA130_assertion
{
miriam-gene:338340
a
ncit:C16612
.
lld:C0017097
a
ncit:C7057
.
dgn-gda:DGN5d2685b4cc12e0f9006a6272a4d7d5c8
sio:SIO_000628
miriam-gene:338340
,
lld:C0017097
;
a
sio:SIO_001121
.
}
dgn-np:NP196013.RADbc5Ak9DVrYAIU5cICeQ8oO28vPUBEZzxv3cly2HnbA130_provenance
{
dgn-np:NP196013.RADbc5Ak9DVrYAIU5cICeQ8oO28vPUBEZzxv3cly2HnbA130_assertion
dct:description
"[Fibroblasts from the clinically affected Gardner's syndrome daughter of the proband were significantly more sensitive to MMS treatment, D0 of 0.22 mM (p less than 0.01) versus the normal average D0 of 0.36 mM and a D10 of 0.97 mM (p less than 0.01) versus the normal average.]. 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:6800649
;
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:NP196013.RADbc5Ak9DVrYAIU5cICeQ8oO28vPUBEZzxv3cly2HnbA130_publicationInfo
{
this:
dct:created
"2014-10-02T12:33:48+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}