@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP510562.RAsoVbYiAVATtYwjX8SP-ArIdmFJu4n2IIhvfd5WFeBCM
> .
@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:NP510562.RAsoVbYiAVATtYwjX8SP-ArIdmFJu4n2IIhvfd5WFeBCM130_head
{
this:
np:hasAssertion
dgn-np:NP510562.RAsoVbYiAVATtYwjX8SP-ArIdmFJu4n2IIhvfd5WFeBCM130_assertion
;
np:hasProvenance
dgn-np:NP510562.RAsoVbYiAVATtYwjX8SP-ArIdmFJu4n2IIhvfd5WFeBCM130_provenance
;
np:hasPublicationInfo
dgn-np:NP510562.RAsoVbYiAVATtYwjX8SP-ArIdmFJu4n2IIhvfd5WFeBCM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP510562.RAsoVbYiAVATtYwjX8SP-ArIdmFJu4n2IIhvfd5WFeBCM130_assertion
a
np:Assertion
.
dgn-np:NP510562.RAsoVbYiAVATtYwjX8SP-ArIdmFJu4n2IIhvfd5WFeBCM130_provenance
a
np:Provenance
.
dgn-np:NP510562.RAsoVbYiAVATtYwjX8SP-ArIdmFJu4n2IIhvfd5WFeBCM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP510562.RAsoVbYiAVATtYwjX8SP-ArIdmFJu4n2IIhvfd5WFeBCM130_assertion
{
miriam-gene:2572
a
ncit:C16612
.
lld:C0028756
a
ncit:C7057
.
dgn-gda:DGN324d29302ba03bb3ce0da35dcb0f2201
sio:SIO_000628
miriam-gene:2572
,
lld:C0028756
;
a
sio:SIO_001121
.
}
dgn-np:NP510562.RAsoVbYiAVATtYwjX8SP-ArIdmFJu4n2IIhvfd5WFeBCM130_provenance
{
dgn-np:NP510562.RAsoVbYiAVATtYwjX8SP-ArIdmFJu4n2IIhvfd5WFeBCM130_assertion
dcterms:description
"[Potential confounding variables in association studies involving common variants and complex diseases (low power to detect modest genetic effects, overinterpretation of marginal data, population stratification, and biological plausibility) are also discussed in the context of GAD2 and severe obesity.]. 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:16122350
;
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:NP510562.RAsoVbYiAVATtYwjX8SP-ArIdmFJu4n2IIhvfd5WFeBCM130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:36+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" .
}