@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP59961.RAemq66TGvYxPTBwsSuIhvfi-t9xZOH7n5So_DZ_IcUJU
> .
@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:NP59961.RAemq66TGvYxPTBwsSuIhvfi-t9xZOH7n5So_DZ_IcUJU130_head
{
this:
np:hasAssertion
dgn-np:NP59961.RAemq66TGvYxPTBwsSuIhvfi-t9xZOH7n5So_DZ_IcUJU130_assertion
;
np:hasProvenance
dgn-np:NP59961.RAemq66TGvYxPTBwsSuIhvfi-t9xZOH7n5So_DZ_IcUJU130_provenance
;
np:hasPublicationInfo
dgn-np:NP59961.RAemq66TGvYxPTBwsSuIhvfi-t9xZOH7n5So_DZ_IcUJU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP59961.RAemq66TGvYxPTBwsSuIhvfi-t9xZOH7n5So_DZ_IcUJU130_assertion
a
np:Assertion
.
dgn-np:NP59961.RAemq66TGvYxPTBwsSuIhvfi-t9xZOH7n5So_DZ_IcUJU130_provenance
a
np:Provenance
.
dgn-np:NP59961.RAemq66TGvYxPTBwsSuIhvfi-t9xZOH7n5So_DZ_IcUJU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP59961.RAemq66TGvYxPTBwsSuIhvfi-t9xZOH7n5So_DZ_IcUJU130_assertion
{
miriam-gene:1375
a
ncit:C16612
.
lld:C0149721
a
ncit:C7057
.
dgn-gda:DGNfbc2f9b6bcb0fd96600d279efeefeb6f
sio:SIO_000628
miriam-gene:1375
,
lld:C0149721
;
a
sio:SIO_001122
.
}
dgn-np:NP59961.RAemq66TGvYxPTBwsSuIhvfi-t9xZOH7n5So_DZ_IcUJU130_provenance
{
dgn-np:NP59961.RAemq66TGvYxPTBwsSuIhvfi-t9xZOH7n5So_DZ_IcUJU130_assertion
dcterms:description
"[ These results identify the carnitine-transporter gene family as candidate modifiers of LVMI in human hypertension. The use of common SNPs to define informative haplotypes associated with the phenotype of interest is the starting point for progress toward identification of the trapped contributing SNP(s).]. 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:15647998
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP59961.RAemq66TGvYxPTBwsSuIhvfi-t9xZOH7n5So_DZ_IcUJU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:28+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" .
}