@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP195416.RA6Zpl1NxJr2ZJ0T6fYQTMq829AE8q7ak2A6zyQD_w0LE
> .
@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:NP195416.RA6Zpl1NxJr2ZJ0T6fYQTMq829AE8q7ak2A6zyQD_w0LE130_head
{
this:
np:hasAssertion
dgn-np:NP195416.RA6Zpl1NxJr2ZJ0T6fYQTMq829AE8q7ak2A6zyQD_w0LE130_assertion
;
np:hasProvenance
dgn-np:NP195416.RA6Zpl1NxJr2ZJ0T6fYQTMq829AE8q7ak2A6zyQD_w0LE130_provenance
;
np:hasPublicationInfo
dgn-np:NP195416.RA6Zpl1NxJr2ZJ0T6fYQTMq829AE8q7ak2A6zyQD_w0LE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP195416.RA6Zpl1NxJr2ZJ0T6fYQTMq829AE8q7ak2A6zyQD_w0LE130_assertion
a
np:Assertion
.
dgn-np:NP195416.RA6Zpl1NxJr2ZJ0T6fYQTMq829AE8q7ak2A6zyQD_w0LE130_provenance
a
np:Provenance
.
dgn-np:NP195416.RA6Zpl1NxJr2ZJ0T6fYQTMq829AE8q7ak2A6zyQD_w0LE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP195416.RA6Zpl1NxJr2ZJ0T6fYQTMq829AE8q7ak2A6zyQD_w0LE130_assertion
{
miriam-gene:51741
a
ncit:C16612
.
lld:C0007115
a
ncit:C7057
.
dgn-gda:DGN2fbb2d98df203714132cce65c6b90479
sio:SIO_000628
miriam-gene:51741
,
lld:C0007115
;
a
sio:SIO_001121
.
}
dgn-np:NP195416.RA6Zpl1NxJr2ZJ0T6fYQTMq829AE8q7ak2A6zyQD_w0LE130_provenance
{
dgn-np:NP195416.RA6Zpl1NxJr2ZJ0T6fYQTMq829AE8q7ak2A6zyQD_w0LE130_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:NP195416.RA6Zpl1NxJr2ZJ0T6fYQTMq829AE8q7ak2A6zyQD_w0LE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:47+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" .
}