@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP797568.RAqC_Vwyy8NP0R02gTZMRSTfCTyD4b3LEsNuFA7pis-Tc
> .
@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:NP797568.RAqC_Vwyy8NP0R02gTZMRSTfCTyD4b3LEsNuFA7pis-Tc130_head
{
this:
np:hasAssertion
dgn-np:NP797568.RAqC_Vwyy8NP0R02gTZMRSTfCTyD4b3LEsNuFA7pis-Tc130_assertion
;
np:hasProvenance
dgn-np:NP797568.RAqC_Vwyy8NP0R02gTZMRSTfCTyD4b3LEsNuFA7pis-Tc130_provenance
;
np:hasPublicationInfo
dgn-np:NP797568.RAqC_Vwyy8NP0R02gTZMRSTfCTyD4b3LEsNuFA7pis-Tc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP797568.RAqC_Vwyy8NP0R02gTZMRSTfCTyD4b3LEsNuFA7pis-Tc130_assertion
a
np:Assertion
.
dgn-np:NP797568.RAqC_Vwyy8NP0R02gTZMRSTfCTyD4b3LEsNuFA7pis-Tc130_provenance
a
np:Provenance
.
dgn-np:NP797568.RAqC_Vwyy8NP0R02gTZMRSTfCTyD4b3LEsNuFA7pis-Tc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP797568.RAqC_Vwyy8NP0R02gTZMRSTfCTyD4b3LEsNuFA7pis-Tc130_assertion
{
miriam-gene:4129
a
ncit:C16612
.
lld:C0162429
a
ncit:C7057
.
dgn-gda:DGNce1b310ddcc2883472051af7137c2b11
sio:SIO_000628
miriam-gene:4129
,
lld:C0162429
;
a
sio:SIO_001121
.
}
dgn-np:NP797568.RAqC_Vwyy8NP0R02gTZMRSTfCTyD4b3LEsNuFA7pis-Tc130_provenance
{
dgn-np:NP797568.RAqC_Vwyy8NP0R02gTZMRSTfCTyD4b3LEsNuFA7pis-Tc130_assertion
dcterms:description
"[Issues that remain to be resolved are the function of the NDP gene product, the frequency and phenotype of the MAOA deficiency state, and the possible occurrence and phenotype of an MAOB deficiency state.]. 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:NP797568.RAqC_Vwyy8NP0R02gTZMRSTfCTyD4b3LEsNuFA7pis-Tc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:09+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" .
}