@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP239249.RA_r143ir8jnOc4D6Xa7qeJtvx0TXlSvCXZsi7-HGFJYo
> .
@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:NP239249.RA_r143ir8jnOc4D6Xa7qeJtvx0TXlSvCXZsi7-HGFJYo130_head
{
this:
np:hasAssertion
dgn-np:NP239249.RA_r143ir8jnOc4D6Xa7qeJtvx0TXlSvCXZsi7-HGFJYo130_assertion
;
np:hasProvenance
dgn-np:NP239249.RA_r143ir8jnOc4D6Xa7qeJtvx0TXlSvCXZsi7-HGFJYo130_provenance
;
np:hasPublicationInfo
dgn-np:NP239249.RA_r143ir8jnOc4D6Xa7qeJtvx0TXlSvCXZsi7-HGFJYo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP239249.RA_r143ir8jnOc4D6Xa7qeJtvx0TXlSvCXZsi7-HGFJYo130_assertion
a
np:Assertion
.
dgn-np:NP239249.RA_r143ir8jnOc4D6Xa7qeJtvx0TXlSvCXZsi7-HGFJYo130_provenance
a
np:Provenance
.
dgn-np:NP239249.RA_r143ir8jnOc4D6Xa7qeJtvx0TXlSvCXZsi7-HGFJYo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP239249.RA_r143ir8jnOc4D6Xa7qeJtvx0TXlSvCXZsi7-HGFJYo130_assertion
{
miriam-gene:8897
a
ncit:C16612
.
lld:C0024623
a
ncit:C7057
.
dgn-gda:DGN94f5f76f495ed33acf77416b806c97df
sio:SIO_000628
miriam-gene:8897
,
lld:C0024623
;
a
sio:SIO_001121
.
}
dgn-np:NP239249.RA_r143ir8jnOc4D6Xa7qeJtvx0TXlSvCXZsi7-HGFJYo130_provenance
{
dgn-np:NP239249.RA_r143ir8jnOc4D6Xa7qeJtvx0TXlSvCXZsi7-HGFJYo130_assertion
dcterms:description
"[The CDC14A and MTMR3 mutations detected in the GC and CRC were deletion or duplication mutations of one base in the nucleotide repeats that would result in premature stops of the amino acid syntheses.]. 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:20477815
;
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:NP239249.RA_r143ir8jnOc4D6Xa7qeJtvx0TXlSvCXZsi7-HGFJYo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:14+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" .
}