@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP450057.RAzXypbULCsOxKTvksHpagTpDO9IbDxaoerOfFjfB2nV8
> .
@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:NP450057.RAzXypbULCsOxKTvksHpagTpDO9IbDxaoerOfFjfB2nV8130_head
{
this:
np:hasAssertion
dgn-np:NP450057.RAzXypbULCsOxKTvksHpagTpDO9IbDxaoerOfFjfB2nV8130_assertion
;
np:hasProvenance
dgn-np:NP450057.RAzXypbULCsOxKTvksHpagTpDO9IbDxaoerOfFjfB2nV8130_provenance
;
np:hasPublicationInfo
dgn-np:NP450057.RAzXypbULCsOxKTvksHpagTpDO9IbDxaoerOfFjfB2nV8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP450057.RAzXypbULCsOxKTvksHpagTpDO9IbDxaoerOfFjfB2nV8130_assertion
a
np:Assertion
.
dgn-np:NP450057.RAzXypbULCsOxKTvksHpagTpDO9IbDxaoerOfFjfB2nV8130_provenance
a
np:Provenance
.
dgn-np:NP450057.RAzXypbULCsOxKTvksHpagTpDO9IbDxaoerOfFjfB2nV8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP450057.RAzXypbULCsOxKTvksHpagTpDO9IbDxaoerOfFjfB2nV8130_assertion
{
miriam-gene:3176
a
ncit:C16612
.
lld:C0149931
a
ncit:C7057
.
dgn-gda:DGN34325e306357146f7dfec432d420968b
sio:SIO_000628
miriam-gene:3176
,
lld:C0149931
;
a
sio:SIO_001121
.
}
dgn-np:NP450057.RAzXypbULCsOxKTvksHpagTpDO9IbDxaoerOfFjfB2nV8130_provenance
{
dgn-np:NP450057.RAzXypbULCsOxKTvksHpagTpDO9IbDxaoerOfFjfB2nV8130_assertion
dcterms:description
"[The frequencies of the HNMT genotypes and allelic variants did not differ significantly between migraine patients and controls, and were unrelated with the age of onset of migraine attacks, gender, personal history of allergic diseases, family history of migraine, or presence of aura.]. 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:18266724
;
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:NP450057.RAzXypbULCsOxKTvksHpagTpDO9IbDxaoerOfFjfB2nV8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:28+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" .
}