@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP488493.RAWeJV5lqXL20fmQaUJcDGmzbqiucNcA3H0UEoxXgIBtE
> .
@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:NP488493.RAWeJV5lqXL20fmQaUJcDGmzbqiucNcA3H0UEoxXgIBtE130_head
{
this:
np:hasAssertion
dgn-np:NP488493.RAWeJV5lqXL20fmQaUJcDGmzbqiucNcA3H0UEoxXgIBtE130_assertion
;
np:hasProvenance
dgn-np:NP488493.RAWeJV5lqXL20fmQaUJcDGmzbqiucNcA3H0UEoxXgIBtE130_provenance
;
np:hasPublicationInfo
dgn-np:NP488493.RAWeJV5lqXL20fmQaUJcDGmzbqiucNcA3H0UEoxXgIBtE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP488493.RAWeJV5lqXL20fmQaUJcDGmzbqiucNcA3H0UEoxXgIBtE130_assertion
a
np:Assertion
.
dgn-np:NP488493.RAWeJV5lqXL20fmQaUJcDGmzbqiucNcA3H0UEoxXgIBtE130_provenance
a
np:Provenance
.
dgn-np:NP488493.RAWeJV5lqXL20fmQaUJcDGmzbqiucNcA3H0UEoxXgIBtE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP488493.RAWeJV5lqXL20fmQaUJcDGmzbqiucNcA3H0UEoxXgIBtE130_assertion
{
miriam-gene:4852
a
ncit:C16612
.
lld:C0011860
a
ncit:C7057
.
dgn-gda:DGNc49cdf8166da50b5d9f7feebc692b376
sio:SIO_000628
miriam-gene:4852
,
lld:C0011860
;
a
sio:SIO_001121
.
}
dgn-np:NP488493.RAWeJV5lqXL20fmQaUJcDGmzbqiucNcA3H0UEoxXgIBtE130_provenance
{
dgn-np:NP488493.RAWeJV5lqXL20fmQaUJcDGmzbqiucNcA3H0UEoxXgIBtE130_assertion
dcterms:description
"[The present study thus provides the evidence that Leu7Pro polymorphism in the NPY gene is associated with IGT and T2DM in Swedish men, and indicates that the NPY gene variations contribute to development of T2DM.]. 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:15926114
;
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:NP488493.RAWeJV5lqXL20fmQaUJcDGmzbqiucNcA3H0UEoxXgIBtE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:52+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" .
}