@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP613107.RAc95C5i3V6Mkz2hQUxo-0r6xdFqn5sqfFQb_0EAaqnOI
> .
@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:NP613107.RAc95C5i3V6Mkz2hQUxo-0r6xdFqn5sqfFQb_0EAaqnOI130_head
{
this:
np:hasAssertion
dgn-np:NP613107.RAc95C5i3V6Mkz2hQUxo-0r6xdFqn5sqfFQb_0EAaqnOI130_assertion
;
np:hasProvenance
dgn-np:NP613107.RAc95C5i3V6Mkz2hQUxo-0r6xdFqn5sqfFQb_0EAaqnOI130_provenance
;
np:hasPublicationInfo
dgn-np:NP613107.RAc95C5i3V6Mkz2hQUxo-0r6xdFqn5sqfFQb_0EAaqnOI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP613107.RAc95C5i3V6Mkz2hQUxo-0r6xdFqn5sqfFQb_0EAaqnOI130_assertion
a
np:Assertion
.
dgn-np:NP613107.RAc95C5i3V6Mkz2hQUxo-0r6xdFqn5sqfFQb_0EAaqnOI130_provenance
a
np:Provenance
.
dgn-np:NP613107.RAc95C5i3V6Mkz2hQUxo-0r6xdFqn5sqfFQb_0EAaqnOI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP613107.RAc95C5i3V6Mkz2hQUxo-0r6xdFqn5sqfFQb_0EAaqnOI130_assertion
{
miriam-gene:4986
a
ncit:C16612
.
lld:C2239176
a
ncit:C7057
.
dgn-gda:DGNaa32dbc3a9357338250b6aa6ea309e00
sio:SIO_000628
miriam-gene:4986
,
lld:C2239176
;
a
sio:SIO_001121
.
}
dgn-np:NP613107.RAc95C5i3V6Mkz2hQUxo-0r6xdFqn5sqfFQb_0EAaqnOI130_provenance
{
dgn-np:NP613107.RAc95C5i3V6Mkz2hQUxo-0r6xdFqn5sqfFQb_0EAaqnOI130_assertion
dcterms:description
"[A total of 399 Korean (KOR) people, 111 patients with CH, 95 patients with CIR, 86 patients with HCC, and 107 spontaneously recovery, were genotyped for 16 SNPs of the COL3A1 gene.]. 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:19000145
;
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:NP613107.RAc95C5i3V6Mkz2hQUxo-0r6xdFqn5sqfFQb_0EAaqnOI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:10+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" .
}