@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP463903.RATKUOVR2EyCkn4DlmUVVbNf4pt29EjWWhD8vKJMVFDL4
> .
@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:NP463903.RATKUOVR2EyCkn4DlmUVVbNf4pt29EjWWhD8vKJMVFDL4130_head
{
this:
np:hasAssertion
dgn-np:NP463903.RATKUOVR2EyCkn4DlmUVVbNf4pt29EjWWhD8vKJMVFDL4130_assertion
;
np:hasProvenance
dgn-np:NP463903.RATKUOVR2EyCkn4DlmUVVbNf4pt29EjWWhD8vKJMVFDL4130_provenance
;
np:hasPublicationInfo
dgn-np:NP463903.RATKUOVR2EyCkn4DlmUVVbNf4pt29EjWWhD8vKJMVFDL4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP463903.RATKUOVR2EyCkn4DlmUVVbNf4pt29EjWWhD8vKJMVFDL4130_assertion
a
np:Assertion
.
dgn-np:NP463903.RATKUOVR2EyCkn4DlmUVVbNf4pt29EjWWhD8vKJMVFDL4130_provenance
a
np:Provenance
.
dgn-np:NP463903.RATKUOVR2EyCkn4DlmUVVbNf4pt29EjWWhD8vKJMVFDL4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP463903.RATKUOVR2EyCkn4DlmUVVbNf4pt29EjWWhD8vKJMVFDL4130_assertion
{
miriam-gene:3082
a
ncit:C16612
.
lld:C0577631
a
ncit:C7057
.
dgn-gda:DGN38db74758972e1268b1e60b52267d97d
sio:SIO_000628
miriam-gene:3082
,
lld:C0577631
;
a
sio:SIO_001121
.
}
dgn-np:NP463903.RATKUOVR2EyCkn4DlmUVVbNf4pt29EjWWhD8vKJMVFDL4130_provenance
{
dgn-np:NP463903.RATKUOVR2EyCkn4DlmUVVbNf4pt29EjWWhD8vKJMVFDL4130_assertion
dcterms:description
"[Because the influence of genetic variation of HGF has not been examined, we identified single nucleotide polymorphisms (SNPs) in the HGF gene, and investigated the association between these SNPs and blood pressure or carotid atherosclerosis in the Japanese general population.]. 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:15064106
;
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:NP463903.RATKUOVR2EyCkn4DlmUVVbNf4pt29EjWWhD8vKJMVFDL4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:36+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" .
}