@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP92371.RAJz0gHKHIdPEZzb_Z5DKtP1dRmuBRZB7Ff7_L8F2cVJs
> .
@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:NP92371.RAJz0gHKHIdPEZzb_Z5DKtP1dRmuBRZB7Ff7_L8F2cVJs130_head
{
this:
np:hasAssertion
dgn-np:NP92371.RAJz0gHKHIdPEZzb_Z5DKtP1dRmuBRZB7Ff7_L8F2cVJs130_assertion
;
np:hasProvenance
dgn-np:NP92371.RAJz0gHKHIdPEZzb_Z5DKtP1dRmuBRZB7Ff7_L8F2cVJs130_provenance
;
np:hasPublicationInfo
dgn-np:NP92371.RAJz0gHKHIdPEZzb_Z5DKtP1dRmuBRZB7Ff7_L8F2cVJs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP92371.RAJz0gHKHIdPEZzb_Z5DKtP1dRmuBRZB7Ff7_L8F2cVJs130_assertion
a
np:Assertion
.
dgn-np:NP92371.RAJz0gHKHIdPEZzb_Z5DKtP1dRmuBRZB7Ff7_L8F2cVJs130_provenance
a
np:Provenance
.
dgn-np:NP92371.RAJz0gHKHIdPEZzb_Z5DKtP1dRmuBRZB7Ff7_L8F2cVJs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP92371.RAJz0gHKHIdPEZzb_Z5DKtP1dRmuBRZB7Ff7_L8F2cVJs130_assertion
{
miriam-gene:6532
a
ncit:C16612
.
lld:C0851578
a
ncit:C7057
.
dgn-gda:DGNefa31f52cfb3bbbbc30096b5a1f2f45f
sio:SIO_000628
miriam-gene:6532
,
lld:C0851578
;
a
sio:SIO_001122
.
}
dgn-np:NP92371.RAJz0gHKHIdPEZzb_Z5DKtP1dRmuBRZB7Ff7_L8F2cVJs130_provenance
{
dgn-np:NP92371.RAJz0gHKHIdPEZzb_Z5DKtP1dRmuBRZB7Ff7_L8F2cVJs130_assertion
dcterms:description
"[ STG polymorphism appears to be associated with the occurrence of OSAS, especially in male patients. Absence of association of between genetic variants and polysomnography findings may suggest that some mechanisms other than STG polymorphism are involved ]. 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:15867649
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP92371.RAJz0gHKHIdPEZzb_Z5DKtP1dRmuBRZB7Ff7_L8F2cVJs130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:42:30+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" .
}