@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP295785.RAcWv6rzpOZjKkUFiio6HWToyeMChteOImvO-YgKtMHAg
> .
@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:NP295785.RAcWv6rzpOZjKkUFiio6HWToyeMChteOImvO-YgKtMHAg130_head
{
this:
np:hasAssertion
dgn-np:NP295785.RAcWv6rzpOZjKkUFiio6HWToyeMChteOImvO-YgKtMHAg130_assertion
;
np:hasProvenance
dgn-np:NP295785.RAcWv6rzpOZjKkUFiio6HWToyeMChteOImvO-YgKtMHAg130_provenance
;
np:hasPublicationInfo
dgn-np:NP295785.RAcWv6rzpOZjKkUFiio6HWToyeMChteOImvO-YgKtMHAg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP295785.RAcWv6rzpOZjKkUFiio6HWToyeMChteOImvO-YgKtMHAg130_assertion
a
np:Assertion
.
dgn-np:NP295785.RAcWv6rzpOZjKkUFiio6HWToyeMChteOImvO-YgKtMHAg130_provenance
a
np:Provenance
.
dgn-np:NP295785.RAcWv6rzpOZjKkUFiio6HWToyeMChteOImvO-YgKtMHAg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP295785.RAcWv6rzpOZjKkUFiio6HWToyeMChteOImvO-YgKtMHAg130_assertion
{
miriam-gene:3623
a
ncit:C16612
.
lld:C0027651
a
ncit:C7057
.
dgn-gda:DGN94b2f86e089df9149fb692fd0b0b2c8a
sio:SIO_000628
miriam-gene:3623
,
lld:C0027651
;
a
sio:SIO_001121
.
}
dgn-np:NP295785.RAcWv6rzpOZjKkUFiio6HWToyeMChteOImvO-YgKtMHAg130_provenance
{
dgn-np:NP295785.RAcWv6rzpOZjKkUFiio6HWToyeMChteOImvO-YgKtMHAg130_assertion
dcterms:description
"[We conclude that these sequence alterations and the detected 2q allelic changes suggest that INHA may be one of the contributing factors needed for ACT formation in pediatric patient carriers of the R337H TP53 mutation.]. 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:15121773
;
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:NP295785.RAcWv6rzpOZjKkUFiio6HWToyeMChteOImvO-YgKtMHAg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:48+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" .
}