@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP539423.RAo-DSBHPrHIUVWGSBqENhx3zSjqxHcRCfz4wqr_4LGYI
> .
@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:NP539423.RAo-DSBHPrHIUVWGSBqENhx3zSjqxHcRCfz4wqr_4LGYI130_head
{
this:
np:hasAssertion
dgn-np:NP539423.RAo-DSBHPrHIUVWGSBqENhx3zSjqxHcRCfz4wqr_4LGYI130_assertion
;
np:hasProvenance
dgn-np:NP539423.RAo-DSBHPrHIUVWGSBqENhx3zSjqxHcRCfz4wqr_4LGYI130_provenance
;
np:hasPublicationInfo
dgn-np:NP539423.RAo-DSBHPrHIUVWGSBqENhx3zSjqxHcRCfz4wqr_4LGYI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP539423.RAo-DSBHPrHIUVWGSBqENhx3zSjqxHcRCfz4wqr_4LGYI130_assertion
a
np:Assertion
.
dgn-np:NP539423.RAo-DSBHPrHIUVWGSBqENhx3zSjqxHcRCfz4wqr_4LGYI130_provenance
a
np:Provenance
.
dgn-np:NP539423.RAo-DSBHPrHIUVWGSBqENhx3zSjqxHcRCfz4wqr_4LGYI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP539423.RAo-DSBHPrHIUVWGSBqENhx3zSjqxHcRCfz4wqr_4LGYI130_assertion
{
miriam-gene:2549
a
ncit:C16612
.
lld:C0850666
a
ncit:C7057
.
dgn-gda:DGNee820b5f7b4cb2ef659987f9c6ee3608
sio:SIO_000628
miriam-gene:2549
,
lld:C0850666
;
a
sio:SIO_001121
.
}
dgn-np:NP539423.RAo-DSBHPrHIUVWGSBqENhx3zSjqxHcRCfz4wqr_4LGYI130_provenance
{
dgn-np:NP539423.RAo-DSBHPrHIUVWGSBqENhx3zSjqxHcRCfz4wqr_4LGYI130_assertion
dcterms:description
"[This study represents that the Gab1 polymorphism was associated with the low risk of H. pylori infection and the high risk of gastric atrophy among seropositive healthy controls, and that seropositive individuals with PTPN11 G/G and Gab1 G/A+G/G were associated with the greatest risk of gastric atrophy.]. 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:17211494
;
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:NP539423.RAo-DSBHPrHIUVWGSBqENhx3zSjqxHcRCfz4wqr_4LGYI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:25+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" .
}