@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP77043.RA6l7DNRO0-XLtzyCY5Bq-78LHCaqhrM9Av9XZDkLHZFk
> .
@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:NP77043.RA6l7DNRO0-XLtzyCY5Bq-78LHCaqhrM9Av9XZDkLHZFk130_head
{
this:
np:hasAssertion
dgn-np:NP77043.RA6l7DNRO0-XLtzyCY5Bq-78LHCaqhrM9Av9XZDkLHZFk130_assertion
;
np:hasProvenance
dgn-np:NP77043.RA6l7DNRO0-XLtzyCY5Bq-78LHCaqhrM9Av9XZDkLHZFk130_provenance
;
np:hasPublicationInfo
dgn-np:NP77043.RA6l7DNRO0-XLtzyCY5Bq-78LHCaqhrM9Av9XZDkLHZFk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP77043.RA6l7DNRO0-XLtzyCY5Bq-78LHCaqhrM9Av9XZDkLHZFk130_assertion
a
np:Assertion
.
dgn-np:NP77043.RA6l7DNRO0-XLtzyCY5Bq-78LHCaqhrM9Av9XZDkLHZFk130_provenance
a
np:Provenance
.
dgn-np:NP77043.RA6l7DNRO0-XLtzyCY5Bq-78LHCaqhrM9Av9XZDkLHZFk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP77043.RA6l7DNRO0-XLtzyCY5Bq-78LHCaqhrM9Av9XZDkLHZFk130_assertion
{
miriam-gene:3274
a
ncit:C16612
.
lld:C0036341
a
ncit:C7057
.
dgn-gda:DGN2335da9579e79ec77efd313d5fb3de5a
sio:SIO_000628
miriam-gene:3274
,
lld:C0036341
;
a
sio:SIO_001122
.
}
dgn-np:NP77043.RA6l7DNRO0-XLtzyCY5Bq-78LHCaqhrM9Av9XZDkLHZFk130_provenance
{
dgn-np:NP77043.RA6l7DNRO0-XLtzyCY5Bq-78LHCaqhrM9Av9XZDkLHZFk130_assertion
dcterms:description
"[We have concluded that the participation of these variants in the disorder is unlikely, particularly in view of their apparent lack of function and unlikely influence on receptor expression. However their nature alludes to the potential presence of other ]. 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:12429384
;
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:NP77043.RA6l7DNRO0-XLtzyCY5Bq-78LHCaqhrM9Av9XZDkLHZFk130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:42:23+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" .
}