@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP758952.RAhuHCeRbXdYjH-CGU05nJKo7MnFmpNqv0wa8G5WW2JC4
> .
@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:NP758952.RAhuHCeRbXdYjH-CGU05nJKo7MnFmpNqv0wa8G5WW2JC4130_head
{
this:
np:hasAssertion
dgn-np:NP758952.RAhuHCeRbXdYjH-CGU05nJKo7MnFmpNqv0wa8G5WW2JC4130_assertion
;
np:hasProvenance
dgn-np:NP758952.RAhuHCeRbXdYjH-CGU05nJKo7MnFmpNqv0wa8G5WW2JC4130_provenance
;
np:hasPublicationInfo
dgn-np:NP758952.RAhuHCeRbXdYjH-CGU05nJKo7MnFmpNqv0wa8G5WW2JC4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP758952.RAhuHCeRbXdYjH-CGU05nJKo7MnFmpNqv0wa8G5WW2JC4130_assertion
a
np:Assertion
.
dgn-np:NP758952.RAhuHCeRbXdYjH-CGU05nJKo7MnFmpNqv0wa8G5WW2JC4130_provenance
a
np:Provenance
.
dgn-np:NP758952.RAhuHCeRbXdYjH-CGU05nJKo7MnFmpNqv0wa8G5WW2JC4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP758952.RAhuHCeRbXdYjH-CGU05nJKo7MnFmpNqv0wa8G5WW2JC4130_assertion
{
miriam-gene:2004
a
ncit:C16612
.
lld:C1263846
a
ncit:C7057
.
dgn-gda:DGNebd2ae4074f1b6a6c60d5a04295f4407
sio:SIO_000628
miriam-gene:2004
,
lld:C1263846
;
a
sio:SIO_001121
.
}
dgn-np:NP758952.RAhuHCeRbXdYjH-CGU05nJKo7MnFmpNqv0wa8G5WW2JC4130_provenance
{
dgn-np:NP758952.RAhuHCeRbXdYjH-CGU05nJKo7MnFmpNqv0wa8G5WW2JC4130_assertion
dcterms:description
"[Identification of polymorphic sites within NET, specifically those that produce functional consequences, is one critical step in elucidating the genetic variation contributing to the heritable component of diseases such as ADHD.]. 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:19698724
;
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:NP758952.RAhuHCeRbXdYjH-CGU05nJKo7MnFmpNqv0wa8G5WW2JC4130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:29+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" .
}