@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP382638.RAb1B3EcyI052P2rfisKW87C4gNehVk_auR5ewm4UgfG0
> .
@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/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@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/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP382638.RAb1B3EcyI052P2rfisKW87C4gNehVk_auR5ewm4UgfG0130_head
{
this:
np:hasAssertion
dgn-np:NP382638.RAb1B3EcyI052P2rfisKW87C4gNehVk_auR5ewm4UgfG0130_assertion
;
np:hasProvenance
dgn-np:NP382638.RAb1B3EcyI052P2rfisKW87C4gNehVk_auR5ewm4UgfG0130_provenance
;
np:hasPublicationInfo
dgn-np:NP382638.RAb1B3EcyI052P2rfisKW87C4gNehVk_auR5ewm4UgfG0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP382638.RAb1B3EcyI052P2rfisKW87C4gNehVk_auR5ewm4UgfG0130_assertion
a
np:Assertion
.
dgn-np:NP382638.RAb1B3EcyI052P2rfisKW87C4gNehVk_auR5ewm4UgfG0130_provenance
a
np:Provenance
.
dgn-np:NP382638.RAb1B3EcyI052P2rfisKW87C4gNehVk_auR5ewm4UgfG0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP382638.RAb1B3EcyI052P2rfisKW87C4gNehVk_auR5ewm4UgfG0130_assertion
{
miriam-gene:9132
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN13bd419a7512f7c1179a72c6b5d7bbd8
sio:SIO_000628
miriam-gene:9132
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP382638.RAb1B3EcyI052P2rfisKW87C4gNehVk_auR5ewm4UgfG0130_provenance
{
dgn-np:NP382638.RAb1B3EcyI052P2rfisKW87C4gNehVk_auR5ewm4UgfG0130_assertion
dcterms:description
"[These SNPs are in or near genes that are highly expressed in the brain (HECW2, HIP1, BIN2, GRIA1), genes involved in neural development and function (KCNQ4, LMO4, GRIA1, NETO1) and autophagy (ATG4C), and genes that are associated with risk of various diseases including cancer and Alzheimer's disease.]. 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:21782286
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP382638.RAb1B3EcyI052P2rfisKW87C4gNehVk_auR5ewm4UgfG0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:46+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:disgenetrdf
;
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
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}