@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP407050.RAqwR8IHOh0XXbT68gp_JjwBhY5SwjRm9cbPwTuafSYo8
> .
@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:NP407050.RAqwR8IHOh0XXbT68gp_JjwBhY5SwjRm9cbPwTuafSYo8130_head
{
this:
np:hasAssertion
dgn-np:NP407050.RAqwR8IHOh0XXbT68gp_JjwBhY5SwjRm9cbPwTuafSYo8130_assertion
;
np:hasProvenance
dgn-np:NP407050.RAqwR8IHOh0XXbT68gp_JjwBhY5SwjRm9cbPwTuafSYo8130_provenance
;
np:hasPublicationInfo
dgn-np:NP407050.RAqwR8IHOh0XXbT68gp_JjwBhY5SwjRm9cbPwTuafSYo8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP407050.RAqwR8IHOh0XXbT68gp_JjwBhY5SwjRm9cbPwTuafSYo8130_assertion
a
np:Assertion
.
dgn-np:NP407050.RAqwR8IHOh0XXbT68gp_JjwBhY5SwjRm9cbPwTuafSYo8130_provenance
a
np:Provenance
.
dgn-np:NP407050.RAqwR8IHOh0XXbT68gp_JjwBhY5SwjRm9cbPwTuafSYo8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP407050.RAqwR8IHOh0XXbT68gp_JjwBhY5SwjRm9cbPwTuafSYo8130_assertion
{
miriam-gene:3091
a
ncit:C16612
.
lld:C0600139
a
ncit:C7057
.
dgn-gda:DGN116d88e0baabd199971c7d84d7056ca4
sio:SIO_000628
miriam-gene:3091
,
lld:C0600139
;
a
sio:SIO_001121
.
}
dgn-np:NP407050.RAqwR8IHOh0XXbT68gp_JjwBhY5SwjRm9cbPwTuafSYo8130_provenance
{
dgn-np:NP407050.RAqwR8IHOh0XXbT68gp_JjwBhY5SwjRm9cbPwTuafSYo8130_assertion
dcterms:description
"[The current findings suggest that HIF1A P582S polymorphism correlates with urinary cancers risk in Caucasian population, while A588T polymorphism may increase the risk of urinary cancers in Asian population and prostate 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:23723982
;
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:NP407050.RAqwR8IHOh0XXbT68gp_JjwBhY5SwjRm9cbPwTuafSYo8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:02+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" .
}