@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP70381.RAQFRdWADHDiPYAxAi5Jt7vwZsNkep6GA4Cgsy1Gx-W2o
> .
@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 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:NP70381.RAQFRdWADHDiPYAxAi5Jt7vwZsNkep6GA4Cgsy1Gx-W2o130_head
{
this:
np:hasAssertion
dgn-np:NP70381.RAQFRdWADHDiPYAxAi5Jt7vwZsNkep6GA4Cgsy1Gx-W2o130_assertion
;
np:hasProvenance
dgn-np:NP70381.RAQFRdWADHDiPYAxAi5Jt7vwZsNkep6GA4Cgsy1Gx-W2o130_provenance
;
np:hasPublicationInfo
dgn-np:NP70381.RAQFRdWADHDiPYAxAi5Jt7vwZsNkep6GA4Cgsy1Gx-W2o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP70381.RAQFRdWADHDiPYAxAi5Jt7vwZsNkep6GA4Cgsy1Gx-W2o130_assertion
a
np:Assertion
.
dgn-np:NP70381.RAQFRdWADHDiPYAxAi5Jt7vwZsNkep6GA4Cgsy1Gx-W2o130_provenance
a
np:Provenance
.
dgn-np:NP70381.RAQFRdWADHDiPYAxAi5Jt7vwZsNkep6GA4Cgsy1Gx-W2o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP70381.RAQFRdWADHDiPYAxAi5Jt7vwZsNkep6GA4Cgsy1Gx-W2o130_assertion
{
miriam-gene:89866
a
ncit:C16612
.
lld:C0028754
a
ncit:C7057
.
dgn-gda:DGN6821cbd36982e9289c40c725755d5d37
sio:SIO_000628
miriam-gene:89866
,
lld:C0028754
;
a
sio:SIO_001122
.
}
dgn-np:NP70381.RAQFRdWADHDiPYAxAi5Jt7vwZsNkep6GA4Cgsy1Gx-W2o130_provenance
{
dgn-np:NP70381.RAQFRdWADHDiPYAxAi5Jt7vwZsNkep6GA4Cgsy1Gx-W2o130_assertion
dct:description
"[The results demonstrated that genetic variation in KCNJ11, BDNF, PFKP, PTER and SEC16B were associated with SGA and support the concept that genetic factors associated with obesity and/or type 2 diabetes are more prevalent in those born SGA compared to those born AGA. We have previously determined that environmental factors are associated with differences in birthweight in the ABC study and now we have demonstrated a significant genetic contribution, suggesting that the interaction between genetics and the environment are important.]. 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:20712903
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
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:NP70381.RAQFRdWADHDiPYAxAi5Jt7vwZsNkep6GA4Cgsy1Gx-W2o130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:34+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}