@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP487303.RAIL2wqHlmvJING77YXX0vHOOd_uxFeK7yJem9Zs-VcLc
> .
@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:NP487303.RAIL2wqHlmvJING77YXX0vHOOd_uxFeK7yJem9Zs-VcLc130_head
{
this:
np:hasAssertion
dgn-np:NP487303.RAIL2wqHlmvJING77YXX0vHOOd_uxFeK7yJem9Zs-VcLc130_assertion
;
np:hasProvenance
dgn-np:NP487303.RAIL2wqHlmvJING77YXX0vHOOd_uxFeK7yJem9Zs-VcLc130_provenance
;
np:hasPublicationInfo
dgn-np:NP487303.RAIL2wqHlmvJING77YXX0vHOOd_uxFeK7yJem9Zs-VcLc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP487303.RAIL2wqHlmvJING77YXX0vHOOd_uxFeK7yJem9Zs-VcLc130_assertion
a
np:Assertion
.
dgn-np:NP487303.RAIL2wqHlmvJING77YXX0vHOOd_uxFeK7yJem9Zs-VcLc130_provenance
a
np:Provenance
.
dgn-np:NP487303.RAIL2wqHlmvJING77YXX0vHOOd_uxFeK7yJem9Zs-VcLc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP487303.RAIL2wqHlmvJING77YXX0vHOOd_uxFeK7yJem9Zs-VcLc130_assertion
{
miriam-gene:4128
a
ncit:C16612
.
lld:C0011570
a
ncit:C7057
.
dgn-gda:DGN86e0a6de37e84bbfa3635fc735da1f5f
sio:SIO_000628
miriam-gene:4128
,
lld:C0011570
;
a
sio:SIO_001121
.
}
dgn-np:NP487303.RAIL2wqHlmvJING77YXX0vHOOd_uxFeK7yJem9Zs-VcLc130_provenance
{
dgn-np:NP487303.RAIL2wqHlmvJING77YXX0vHOOd_uxFeK7yJem9Zs-VcLc130_assertion
dcterms:description
"[The MAOA uVNTR polymorphism has been documented to affect the MAOA gene at the transcriptional level and is associated with aggressive impulsive behaviors, depression associated with suicide (depressed suicide), and major depressive disorder (MDD).]. 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:21605465
;
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:NP487303.RAIL2wqHlmvJING77YXX0vHOOd_uxFeK7yJem9Zs-VcLc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:51+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" .
}