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http://rdf.disgenet.org/nanopublications.trig#NP96654.RADxevKHDLkOuOQWPzVliQ-bigz1DXqiNIyWX2crnCUUc
> .
@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:NP96654.RADxevKHDLkOuOQWPzVliQ-bigz1DXqiNIyWX2crnCUUc130_head
{
this:
np:hasAssertion
dgn-np:NP96654.RADxevKHDLkOuOQWPzVliQ-bigz1DXqiNIyWX2crnCUUc130_assertion
;
np:hasProvenance
dgn-np:NP96654.RADxevKHDLkOuOQWPzVliQ-bigz1DXqiNIyWX2crnCUUc130_provenance
;
np:hasPublicationInfo
dgn-np:NP96654.RADxevKHDLkOuOQWPzVliQ-bigz1DXqiNIyWX2crnCUUc130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP96654.RADxevKHDLkOuOQWPzVliQ-bigz1DXqiNIyWX2crnCUUc130_assertion
a
np:Assertion
.
dgn-np:NP96654.RADxevKHDLkOuOQWPzVliQ-bigz1DXqiNIyWX2crnCUUc130_provenance
a
np:Provenance
.
dgn-np:NP96654.RADxevKHDLkOuOQWPzVliQ-bigz1DXqiNIyWX2crnCUUc130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:653247
a
ncit:C16612
.
lld:C0030297
a
ncit:C7057
.
dgn-gda:DGN674d1ab137d774eee5ff4e3a84d65422
sio:SIO_000628
miriam-gene:653247
,
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;
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.
}
dgn-np:NP96654.RADxevKHDLkOuOQWPzVliQ-bigz1DXqiNIyWX2crnCUUc130_provenance
{
dgn-np:NP96654.RADxevKHDLkOuOQWPzVliQ-bigz1DXqiNIyWX2crnCUUc130_assertion
dcterms:description
"[The variant 161R form of IL-17F is a natural antagonist of the antiangiogenic effects of wild-type 161H IL-17F, and angiogenesis may play an important role in the metastatic spread of pancreatic cancer. In this preliminary study, we hypothesize that the angiogenetic potential of pancreatic cancers in patients with variant IL-17F is higher than that of tumors in patients with wild-type IL-17F, conferring worse prognosis. This exploratory GWAS may provide the foundation for testing the biology and clinical effects of novel genes and their heritable variants through mechanistic and confirmatory studies in pancreatic cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:22142827
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dgn-void:gad-20130706
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prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP96654.RADxevKHDLkOuOQWPzVliQ-bigz1DXqiNIyWX2crnCUUc130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
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http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
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;
prv:usedData
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> , <
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> , <
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http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
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