@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP576976.RA180NXIcrsM_UxUa7Xt_xTse4g40MFstSbAmvMomVX9w
> .
@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:NP576976.RA180NXIcrsM_UxUa7Xt_xTse4g40MFstSbAmvMomVX9w130_head
{
this:
np:hasAssertion
dgn-np:NP576976.RA180NXIcrsM_UxUa7Xt_xTse4g40MFstSbAmvMomVX9w130_assertion
;
np:hasProvenance
dgn-np:NP576976.RA180NXIcrsM_UxUa7Xt_xTse4g40MFstSbAmvMomVX9w130_provenance
;
np:hasPublicationInfo
dgn-np:NP576976.RA180NXIcrsM_UxUa7Xt_xTse4g40MFstSbAmvMomVX9w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP576976.RA180NXIcrsM_UxUa7Xt_xTse4g40MFstSbAmvMomVX9w130_assertion
a
np:Assertion
.
dgn-np:NP576976.RA180NXIcrsM_UxUa7Xt_xTse4g40MFstSbAmvMomVX9w130_provenance
a
np:Provenance
.
dgn-np:NP576976.RA180NXIcrsM_UxUa7Xt_xTse4g40MFstSbAmvMomVX9w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP576976.RA180NXIcrsM_UxUa7Xt_xTse4g40MFstSbAmvMomVX9w130_assertion
{
miriam-gene:3667
a
ncit:C16612
.
lld:C0520679
a
ncit:C7057
.
dgn-gda:DGNb8bbf6a623650b5d7afd176158d4419e
sio:SIO_000628
miriam-gene:3667
,
lld:C0520679
;
a
sio:SIO_001121
.
}
dgn-np:NP576976.RA180NXIcrsM_UxUa7Xt_xTse4g40MFstSbAmvMomVX9w130_provenance
{
dgn-np:NP576976.RA180NXIcrsM_UxUa7Xt_xTse4g40MFstSbAmvMomVX9w130_assertion
dcterms:description
"[The polymorphism of the IRS-1 gene at codon 972, especially Gly/Arg variant, or the presence of the allele for Arg appears to be associated with occurrence of OSAS in male patients, whereas this polymorphism is not related to severity of OSAS.]. 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:17075427
;
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:NP576976.RA180NXIcrsM_UxUa7Xt_xTse4g40MFstSbAmvMomVX9w130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:06+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" .
}