@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP335217.RAcDLBeMheDrjUxKA1-fZWi8Lwjat5ndD0KzWbyHPMY1M
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP335217.RAcDLBeMheDrjUxKA1-fZWi8Lwjat5ndD0KzWbyHPMY1M130_head
{
this:
np:hasAssertion
dgn-np:NP335217.RAcDLBeMheDrjUxKA1-fZWi8Lwjat5ndD0KzWbyHPMY1M130_assertion
;
np:hasProvenance
dgn-np:NP335217.RAcDLBeMheDrjUxKA1-fZWi8Lwjat5ndD0KzWbyHPMY1M130_provenance
;
np:hasPublicationInfo
dgn-np:NP335217.RAcDLBeMheDrjUxKA1-fZWi8Lwjat5ndD0KzWbyHPMY1M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP335217.RAcDLBeMheDrjUxKA1-fZWi8Lwjat5ndD0KzWbyHPMY1M130_assertion
a
np:Assertion
.
dgn-np:NP335217.RAcDLBeMheDrjUxKA1-fZWi8Lwjat5ndD0KzWbyHPMY1M130_provenance
a
np:Provenance
.
dgn-np:NP335217.RAcDLBeMheDrjUxKA1-fZWi8Lwjat5ndD0KzWbyHPMY1M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP335217.RAcDLBeMheDrjUxKA1-fZWi8Lwjat5ndD0KzWbyHPMY1M130_assertion
{
miriam-gene:4846
a
ncit:C16612
.
lld:C0007222
a
ncit:C7057
.
dgn-gda:DGN9634f25ad9c72ac4a7419f558d11587e
sio:SIO_000628
miriam-gene:4846
,
lld:C0007222
;
a
sio:SIO_001121
.
}
dgn-np:NP335217.RAcDLBeMheDrjUxKA1-fZWi8Lwjat5ndD0KzWbyHPMY1M130_provenance
{
dgn-np:NP335217.RAcDLBeMheDrjUxKA1-fZWi8Lwjat5ndD0KzWbyHPMY1M130_assertion
dcterms:description
"[The marked interethnic differences that we found in the distribution of eNOS variants, in the estimated haplotype frequency, and in the association between variants may help us to understand how the combination of these genetic variants may influence cardiovascular diseases.]. 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:11692081
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP335217.RAcDLBeMheDrjUxKA1-fZWi8Lwjat5ndD0KzWbyHPMY1M130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:17+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}