@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP877058.RA7DZwN_rynjp_uSsnIRQQ3rmP6x17sJqN44DHYsY3c8A
> .
@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:NP877058.RA7DZwN_rynjp_uSsnIRQQ3rmP6x17sJqN44DHYsY3c8A130_head
{
this:
np:hasAssertion
dgn-np:NP877058.RA7DZwN_rynjp_uSsnIRQQ3rmP6x17sJqN44DHYsY3c8A130_assertion
;
np:hasProvenance
dgn-np:NP877058.RA7DZwN_rynjp_uSsnIRQQ3rmP6x17sJqN44DHYsY3c8A130_provenance
;
np:hasPublicationInfo
dgn-np:NP877058.RA7DZwN_rynjp_uSsnIRQQ3rmP6x17sJqN44DHYsY3c8A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP877058.RA7DZwN_rynjp_uSsnIRQQ3rmP6x17sJqN44DHYsY3c8A130_assertion
a
np:Assertion
.
dgn-np:NP877058.RA7DZwN_rynjp_uSsnIRQQ3rmP6x17sJqN44DHYsY3c8A130_provenance
a
np:Provenance
.
dgn-np:NP877058.RA7DZwN_rynjp_uSsnIRQQ3rmP6x17sJqN44DHYsY3c8A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP877058.RA7DZwN_rynjp_uSsnIRQQ3rmP6x17sJqN44DHYsY3c8A130_assertion
{
miriam-gene:5340
a
ncit:C16612
.
lld:C0007222
a
ncit:C7057
.
dgn-gda:DGN795835d1bed915fde6f3e12a813a2454
sio:SIO_000628
miriam-gene:5340
,
lld:C0007222
;
a
sio:SIO_001121
.
}
dgn-np:NP877058.RA7DZwN_rynjp_uSsnIRQQ3rmP6x17sJqN44DHYsY3c8A130_provenance
{
dgn-np:NP877058.RA7DZwN_rynjp_uSsnIRQQ3rmP6x17sJqN44DHYsY3c8A130_assertion
dcterms:description
"[The less efficient proteolytic processing of the Pro370Leu protein by plasmin, coupled with the strong association of this variant with ethnicity, suggests that the Pro370Leu CHGA gene variant may contribute to the differential prevalence of cardiovascular disease across ethnic groups.]. 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:17991725
;
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:NP877058.RA7DZwN_rynjp_uSsnIRQQ3rmP6x17sJqN44DHYsY3c8A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:56+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" .
}