@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP672403.RAz3Z7W3K4sH0mmSdgMZ73LdcXaSZbYaDql6dGWN8gGT4
> .
@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:NP672403.RAz3Z7W3K4sH0mmSdgMZ73LdcXaSZbYaDql6dGWN8gGT4130_head
{
this:
np:hasAssertion
dgn-np:NP672403.RAz3Z7W3K4sH0mmSdgMZ73LdcXaSZbYaDql6dGWN8gGT4130_assertion
;
np:hasProvenance
dgn-np:NP672403.RAz3Z7W3K4sH0mmSdgMZ73LdcXaSZbYaDql6dGWN8gGT4130_provenance
;
np:hasPublicationInfo
dgn-np:NP672403.RAz3Z7W3K4sH0mmSdgMZ73LdcXaSZbYaDql6dGWN8gGT4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP672403.RAz3Z7W3K4sH0mmSdgMZ73LdcXaSZbYaDql6dGWN8gGT4130_assertion
a
np:Assertion
.
dgn-np:NP672403.RAz3Z7W3K4sH0mmSdgMZ73LdcXaSZbYaDql6dGWN8gGT4130_provenance
a
np:Provenance
.
dgn-np:NP672403.RAz3Z7W3K4sH0mmSdgMZ73LdcXaSZbYaDql6dGWN8gGT4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP672403.RAz3Z7W3K4sH0mmSdgMZ73LdcXaSZbYaDql6dGWN8gGT4130_assertion
{
miriam-gene:4128
a
ncit:C16612
.
lld:C0162429
a
ncit:C7057
.
dgn-gda:DGN6134d0979b7f038366bf603971bba50f
sio:SIO_000628
miriam-gene:4128
,
lld:C0162429
;
a
sio:SIO_001121
.
}
dgn-np:NP672403.RAz3Z7W3K4sH0mmSdgMZ73LdcXaSZbYaDql6dGWN8gGT4130_provenance
{
dgn-np:NP672403.RAz3Z7W3K4sH0mmSdgMZ73LdcXaSZbYaDql6dGWN8gGT4130_assertion
dcterms:description
"[An MAOA deficiency state has been described in one family to date, with features of altered amine and amine metabolite levels, low normal intelligence, apparent difficulty in impulse control and cardiovascular difficulty in affected males.]. 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:8541872
;
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:NP672403.RAz3Z7W3K4sH0mmSdgMZ73LdcXaSZbYaDql6dGWN8gGT4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:46+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" .
}