@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP718409.RAxYmJ9_oX9-BiEf6cXMPTCzrqVxNkGthgGBMc2_ixgjU
> .
@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:NP718409.RAxYmJ9_oX9-BiEf6cXMPTCzrqVxNkGthgGBMc2_ixgjU130_head
{
this:
np:hasAssertion
dgn-np:NP718409.RAxYmJ9_oX9-BiEf6cXMPTCzrqVxNkGthgGBMc2_ixgjU130_assertion
;
np:hasProvenance
dgn-np:NP718409.RAxYmJ9_oX9-BiEf6cXMPTCzrqVxNkGthgGBMc2_ixgjU130_provenance
;
np:hasPublicationInfo
dgn-np:NP718409.RAxYmJ9_oX9-BiEf6cXMPTCzrqVxNkGthgGBMc2_ixgjU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP718409.RAxYmJ9_oX9-BiEf6cXMPTCzrqVxNkGthgGBMc2_ixgjU130_assertion
a
np:Assertion
.
dgn-np:NP718409.RAxYmJ9_oX9-BiEf6cXMPTCzrqVxNkGthgGBMc2_ixgjU130_provenance
a
np:Provenance
.
dgn-np:NP718409.RAxYmJ9_oX9-BiEf6cXMPTCzrqVxNkGthgGBMc2_ixgjU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP718409.RAxYmJ9_oX9-BiEf6cXMPTCzrqVxNkGthgGBMc2_ixgjU130_assertion
{
miriam-gene:773
a
ncit:C16612
.
lld:C0338480
a
ncit:C7057
.
dgn-gda:DGN1581b0deb9c9eeb3d3a8d03a0db43317
sio:SIO_000628
miriam-gene:773
,
lld:C0338480
;
a
sio:SIO_001121
.
}
dgn-np:NP718409.RAxYmJ9_oX9-BiEf6cXMPTCzrqVxNkGthgGBMc2_ixgjU130_provenance
{
dgn-np:NP718409.RAxYmJ9_oX9-BiEf6cXMPTCzrqVxNkGthgGBMc2_ixgjU130_assertion
dcterms:description
"[The clinical overlap between monogenic Familial Hemiplegic Migraine (FHM) and common migraine subtypes, and the fact that all three FHM genes are involved in the transport of ions, suggest that ion transport genes may underlie susceptibility to common forms of migraine.]. 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:18676988
;
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:NP718409.RAxYmJ9_oX9-BiEf6cXMPTCzrqVxNkGthgGBMc2_ixgjU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:16+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" .
}