@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1144203.RAAVjbeIfRNLD1euIzm6CFSNGi9F7aax6Uv_DLPDGLfnI
> .
@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/
> .
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{
this:
np:hasAssertion
dgn-np:NP1144203.RAAVjbeIfRNLD1euIzm6CFSNGi9F7aax6Uv_DLPDGLfnI130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP1144203.RAAVjbeIfRNLD1euIzm6CFSNGi9F7aax6Uv_DLPDGLfnI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1144203.RAAVjbeIfRNLD1euIzm6CFSNGi9F7aax6Uv_DLPDGLfnI130_assertion
a
np:Assertion
.
dgn-np:NP1144203.RAAVjbeIfRNLD1euIzm6CFSNGi9F7aax6Uv_DLPDGLfnI130_provenance
a
np:Provenance
.
dgn-np:NP1144203.RAAVjbeIfRNLD1euIzm6CFSNGi9F7aax6Uv_DLPDGLfnI130_publicationInfo
a
np:PublicationInfo
.
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dgn-np:NP1144203.RAAVjbeIfRNLD1euIzm6CFSNGi9F7aax6Uv_DLPDGLfnI130_assertion
{
miriam-gene:3953
a
ncit:C16612
.
lld:C0011860
a
ncit:C7057
.
dgn-gda:DGNabf548695a12b47f725bfc495cbeca36
sio:SIO_000628
miriam-gene:3953
,
lld:C0011860
;
a
sio:SIO_001121
.
}
dgn-np:NP1144203.RAAVjbeIfRNLD1euIzm6CFSNGi9F7aax6Uv_DLPDGLfnI130_provenance
{
dgn-np:NP1144203.RAAVjbeIfRNLD1euIzm6CFSNGi9F7aax6Uv_DLPDGLfnI130_assertion
dcterms:description
"[These findings suggest that variants in ADIPOQ and LEPR are risk factors for T2DM and hypertension in the Chinese population and that variants in RETN and TRIB3 are not major risk factors for these diseases.]. 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:24414038
;
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:NP1144203.RAAVjbeIfRNLD1euIzm6CFSNGi9F7aax6Uv_DLPDGLfnI130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:24+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
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;
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" .
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pav:version
"v4.0.0" .
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