@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP51416.RAly7D8UfOgjfDrgpCmerEzh35VQKW_vJ_6VdRDAwB2zs
> .
@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/v3.0.0/void/
> .
dgn-np:NP51416.RAly7D8UfOgjfDrgpCmerEzh35VQKW_vJ_6VdRDAwB2zs130_head
{
this:
np:hasAssertion
dgn-np:NP51416.RAly7D8UfOgjfDrgpCmerEzh35VQKW_vJ_6VdRDAwB2zs130_assertion
;
np:hasProvenance
dgn-np:NP51416.RAly7D8UfOgjfDrgpCmerEzh35VQKW_vJ_6VdRDAwB2zs130_provenance
;
np:hasPublicationInfo
dgn-np:NP51416.RAly7D8UfOgjfDrgpCmerEzh35VQKW_vJ_6VdRDAwB2zs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP51416.RAly7D8UfOgjfDrgpCmerEzh35VQKW_vJ_6VdRDAwB2zs130_assertion
a
np:Assertion
.
dgn-np:NP51416.RAly7D8UfOgjfDrgpCmerEzh35VQKW_vJ_6VdRDAwB2zs130_provenance
a
np:Provenance
.
dgn-np:NP51416.RAly7D8UfOgjfDrgpCmerEzh35VQKW_vJ_6VdRDAwB2zs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP51416.RAly7D8UfOgjfDrgpCmerEzh35VQKW_vJ_6VdRDAwB2zs130_assertion
{
miriam-gene:2784
a
ncit:C16612
.
lld:C0017327
a
ncit:C7057
.
dgn-gda:DGN4c12bce1adfebdf79af5bd1441926bbc
sio:SIO_000628
miriam-gene:2784
,
lld:C0017327
;
a
sio:SIO_001122
.
}
dgn-np:NP51416.RAly7D8UfOgjfDrgpCmerEzh35VQKW_vJ_6VdRDAwB2zs130_provenance
{
dgn-np:NP51416.RAly7D8UfOgjfDrgpCmerEzh35VQKW_vJ_6VdRDAwB2zs130_assertion
dcterms:description
"[Although the effect of the gene on each phenotype appears to be weak, considering the combined impact of the effects of the C825T polymorphism on risk factors, the GNB3 gene may be an important gene for human health.]. 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:15033462
;
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:NP51416.RAly7D8UfOgjfDrgpCmerEzh35VQKW_vJ_6VdRDAwB2zs130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:08+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}