@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP769715.RAVIb8Mg6d29qrMLEX1qz2ecdS26H36WqbvVZAU7TuQrI
> .
@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:NP769715.RAVIb8Mg6d29qrMLEX1qz2ecdS26H36WqbvVZAU7TuQrI130_head
{
this:
np:hasAssertion
dgn-np:NP769715.RAVIb8Mg6d29qrMLEX1qz2ecdS26H36WqbvVZAU7TuQrI130_assertion
;
np:hasProvenance
dgn-np:NP769715.RAVIb8Mg6d29qrMLEX1qz2ecdS26H36WqbvVZAU7TuQrI130_provenance
;
np:hasPublicationInfo
dgn-np:NP769715.RAVIb8Mg6d29qrMLEX1qz2ecdS26H36WqbvVZAU7TuQrI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP769715.RAVIb8Mg6d29qrMLEX1qz2ecdS26H36WqbvVZAU7TuQrI130_assertion
a
np:Assertion
.
dgn-np:NP769715.RAVIb8Mg6d29qrMLEX1qz2ecdS26H36WqbvVZAU7TuQrI130_provenance
a
np:Provenance
.
dgn-np:NP769715.RAVIb8Mg6d29qrMLEX1qz2ecdS26H36WqbvVZAU7TuQrI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP769715.RAVIb8Mg6d29qrMLEX1qz2ecdS26H36WqbvVZAU7TuQrI130_assertion
{
miriam-gene:5300
a
ncit:C16612
.
lld:C1168401
a
ncit:C7057
.
dgn-gda:DGNc869d2b83ba690a530d32b72c18ffc9f
sio:SIO_000628
miriam-gene:5300
,
lld:C1168401
;
a
sio:SIO_001121
.
}
dgn-np:NP769715.RAVIb8Mg6d29qrMLEX1qz2ecdS26H36WqbvVZAU7TuQrI130_provenance
{
dgn-np:NP769715.RAVIb8Mg6d29qrMLEX1qz2ecdS26H36WqbvVZAU7TuQrI130_assertion
dcterms:description
"[In this study, we tested the hypothesis that common polymorphisms in the coding and promoter regions of PIN1 are associated with risk of squamous cell carcinoma of the head and neck (SCCHN).]. 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:19625347
;
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:NP769715.RAVIb8Mg6d29qrMLEX1qz2ecdS26H36WqbvVZAU7TuQrI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:45+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" .
}