@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP212409.RAZMmciG-yXudAzvjJwc8NCc8A5XLFBYUkpwkqp5C6LEE
> .
@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:NP212409.RAZMmciG-yXudAzvjJwc8NCc8A5XLFBYUkpwkqp5C6LEE130_head
{
this:
np:hasAssertion
dgn-np:NP212409.RAZMmciG-yXudAzvjJwc8NCc8A5XLFBYUkpwkqp5C6LEE130_assertion
;
np:hasProvenance
dgn-np:NP212409.RAZMmciG-yXudAzvjJwc8NCc8A5XLFBYUkpwkqp5C6LEE130_provenance
;
np:hasPublicationInfo
dgn-np:NP212409.RAZMmciG-yXudAzvjJwc8NCc8A5XLFBYUkpwkqp5C6LEE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP212409.RAZMmciG-yXudAzvjJwc8NCc8A5XLFBYUkpwkqp5C6LEE130_assertion
a
np:Assertion
.
dgn-np:NP212409.RAZMmciG-yXudAzvjJwc8NCc8A5XLFBYUkpwkqp5C6LEE130_provenance
a
np:Provenance
.
dgn-np:NP212409.RAZMmciG-yXudAzvjJwc8NCc8A5XLFBYUkpwkqp5C6LEE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP212409.RAZMmciG-yXudAzvjJwc8NCc8A5XLFBYUkpwkqp5C6LEE130_assertion
{
miriam-gene:51741
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGNf977fa351524728410240ecad75545d0
sio:SIO_000628
miriam-gene:51741
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP212409.RAZMmciG-yXudAzvjJwc8NCc8A5XLFBYUkpwkqp5C6LEE130_provenance
{
dgn-np:NP212409.RAZMmciG-yXudAzvjJwc8NCc8A5XLFBYUkpwkqp5C6LEE130_assertion
dcterms:description
"[These findings together with other observations from literature on human cancers and the fact that the proline at codon 282 is extremely conserved in phylogenetically distant organisms (including Drosophila) suggest that the variant allele-282 could affect the biological function of WWOX, thereby predisposing individuals to thyroid cancer.]. 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:21520031
;
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:NP212409.RAZMmciG-yXudAzvjJwc8NCc8A5XLFBYUkpwkqp5C6LEE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:58+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" .
}