@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1215998.RAtho1MJHnLbi0-UML4UZNhWX_jPl6X2X-y9ODVSEpMcM
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1215998.RAtho1MJHnLbi0-UML4UZNhWX_jPl6X2X-y9ODVSEpMcM130_head
{
this:
np:hasAssertion
dgn-np:NP1215998.RAtho1MJHnLbi0-UML4UZNhWX_jPl6X2X-y9ODVSEpMcM130_assertion
;
np:hasProvenance
dgn-np:NP1215998.RAtho1MJHnLbi0-UML4UZNhWX_jPl6X2X-y9ODVSEpMcM130_provenance
;
np:hasPublicationInfo
dgn-np:NP1215998.RAtho1MJHnLbi0-UML4UZNhWX_jPl6X2X-y9ODVSEpMcM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1215998.RAtho1MJHnLbi0-UML4UZNhWX_jPl6X2X-y9ODVSEpMcM130_assertion
a
np:Assertion
.
dgn-np:NP1215998.RAtho1MJHnLbi0-UML4UZNhWX_jPl6X2X-y9ODVSEpMcM130_provenance
a
np:Provenance
.
dgn-np:NP1215998.RAtho1MJHnLbi0-UML4UZNhWX_jPl6X2X-y9ODVSEpMcM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1215998.RAtho1MJHnLbi0-UML4UZNhWX_jPl6X2X-y9ODVSEpMcM130_assertion
{
miriam-gene:5027
a
ncit:C16612
.
lld:C0007115
a
ncit:C7057
.
dgn-gda:DGN9d65efde362a5f1f0dc8b4f333a03333
sio:SIO_000628
miriam-gene:5027
,
lld:C0007115
;
a
sio:SIO_001122
.
}
dgn-np:NP1215998.RAtho1MJHnLbi0-UML4UZNhWX_jPl6X2X-y9ODVSEpMcM130_provenance
{
dgn-np:NP1215998.RAtho1MJHnLbi0-UML4UZNhWX_jPl6X2X-y9ODVSEpMcM130_assertion
dcterms:description
"[A polymorphism in exon 13 of the P2X7 receptor gene at the +1513 position (Glu496Ala substitution, corresponding to SNP rs3751143) has been shown to eradicate the function of this receptor and has been correlated with histological variants and clinical parameters in 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:25178922
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1215998.RAtho1MJHnLbi0-UML4UZNhWX_jPl6X2X-y9ODVSEpMcM130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:57+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}