@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP847265.RAUxGFf4dhZtvETTCsvhHvDEsWeGedbHWCDK3zKxN_KgM
> .
@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:NP847265.RAUxGFf4dhZtvETTCsvhHvDEsWeGedbHWCDK3zKxN_KgM130_head
{
this:
np:hasAssertion
dgn-np:NP847265.RAUxGFf4dhZtvETTCsvhHvDEsWeGedbHWCDK3zKxN_KgM130_assertion
;
np:hasProvenance
dgn-np:NP847265.RAUxGFf4dhZtvETTCsvhHvDEsWeGedbHWCDK3zKxN_KgM130_provenance
;
np:hasPublicationInfo
dgn-np:NP847265.RAUxGFf4dhZtvETTCsvhHvDEsWeGedbHWCDK3zKxN_KgM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP847265.RAUxGFf4dhZtvETTCsvhHvDEsWeGedbHWCDK3zKxN_KgM130_assertion
a
np:Assertion
.
dgn-np:NP847265.RAUxGFf4dhZtvETTCsvhHvDEsWeGedbHWCDK3zKxN_KgM130_provenance
a
np:Provenance
.
dgn-np:NP847265.RAUxGFf4dhZtvETTCsvhHvDEsWeGedbHWCDK3zKxN_KgM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP847265.RAUxGFf4dhZtvETTCsvhHvDEsWeGedbHWCDK3zKxN_KgM130_assertion
{
miriam-gene:55349
a
ncit:C16612
.
lld:C0020445
a
ncit:C7057
.
dgn-gda:DGNfed6f94928950a68963471be30e8ee82
sio:SIO_000628
miriam-gene:55349
,
lld:C0020445
;
a
sio:SIO_001121
.
}
dgn-np:NP847265.RAUxGFf4dhZtvETTCsvhHvDEsWeGedbHWCDK3zKxN_KgM130_provenance
{
dgn-np:NP847265.RAUxGFf4dhZtvETTCsvhHvDEsWeGedbHWCDK3zKxN_KgM130_assertion
dcterms:description
"[The main aims of the present work were to determine whether clinical characterization is sufficient to identify these individuals at high risk of developing CHD and to evaluate the clinical applicability of molecular diagnosis for FH.]. 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:20964105
;
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:NP847265.RAUxGFf4dhZtvETTCsvhHvDEsWeGedbHWCDK3zKxN_KgM130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:08+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" .
}