@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP842366.RABD5RNEpC3kdQJbiPvnRWEAfpJj6llnft0F_--2J85ek
> .
@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:NP842366.RABD5RNEpC3kdQJbiPvnRWEAfpJj6llnft0F_--2J85ek130_head
{
this:
np:hasAssertion
dgn-np:NP842366.RABD5RNEpC3kdQJbiPvnRWEAfpJj6llnft0F_--2J85ek130_assertion
;
np:hasProvenance
dgn-np:NP842366.RABD5RNEpC3kdQJbiPvnRWEAfpJj6llnft0F_--2J85ek130_provenance
;
np:hasPublicationInfo
dgn-np:NP842366.RABD5RNEpC3kdQJbiPvnRWEAfpJj6llnft0F_--2J85ek130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP842366.RABD5RNEpC3kdQJbiPvnRWEAfpJj6llnft0F_--2J85ek130_assertion
a
np:Assertion
.
dgn-np:NP842366.RABD5RNEpC3kdQJbiPvnRWEAfpJj6llnft0F_--2J85ek130_provenance
a
np:Provenance
.
dgn-np:NP842366.RABD5RNEpC3kdQJbiPvnRWEAfpJj6llnft0F_--2J85ek130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP842366.RABD5RNEpC3kdQJbiPvnRWEAfpJj6llnft0F_--2J85ek130_assertion
{
miriam-gene:1312
a
ncit:C16612
.
lld:C1863535
a
ncit:C7057
.
dgn-gda:DGN6da008813822fea1744a1bf5719482f8
sio:SIO_000628
miriam-gene:1312
,
lld:C1863535
;
a
sio:SIO_001121
.
}
dgn-np:NP842366.RABD5RNEpC3kdQJbiPvnRWEAfpJj6llnft0F_--2J85ek130_provenance
{
dgn-np:NP842366.RABD5RNEpC3kdQJbiPvnRWEAfpJj6llnft0F_--2J85ek130_assertion
dcterms:description
"[Polymerase chain reaction (PCR) and restriction fragment length polymorphism (RFLP) methods were used to discern the relationships among the functional polymorphism of COMT, mental retardation (MR), and general cognitive ability of children.]. 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:16800379
;
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:NP842366.RABD5RNEpC3kdQJbiPvnRWEAfpJj6llnft0F_--2J85ek130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:35+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" .
}