@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP403905.RAA9x645sUEBpwID9TblsSXBmTozNsMVFF4tC67jfn7xU
> .
@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:NP403905.RAA9x645sUEBpwID9TblsSXBmTozNsMVFF4tC67jfn7xU130_head
{
this:
np:hasAssertion
dgn-np:NP403905.RAA9x645sUEBpwID9TblsSXBmTozNsMVFF4tC67jfn7xU130_assertion
;
np:hasProvenance
dgn-np:NP403905.RAA9x645sUEBpwID9TblsSXBmTozNsMVFF4tC67jfn7xU130_provenance
;
np:hasPublicationInfo
dgn-np:NP403905.RAA9x645sUEBpwID9TblsSXBmTozNsMVFF4tC67jfn7xU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP403905.RAA9x645sUEBpwID9TblsSXBmTozNsMVFF4tC67jfn7xU130_assertion
a
np:Assertion
.
dgn-np:NP403905.RAA9x645sUEBpwID9TblsSXBmTozNsMVFF4tC67jfn7xU130_provenance
a
np:Provenance
.
dgn-np:NP403905.RAA9x645sUEBpwID9TblsSXBmTozNsMVFF4tC67jfn7xU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP403905.RAA9x645sUEBpwID9TblsSXBmTozNsMVFF4tC67jfn7xU130_assertion
{
miriam-gene:7391
a
ncit:C16612
.
lld:C0020474
a
ncit:C7057
.
dgn-gda:DGN1cf8f7c64d22e99f181e8247b8f8fc89
sio:SIO_000628
miriam-gene:7391
,
lld:C0020474
;
a
sio:SIO_001121
.
}
dgn-np:NP403905.RAA9x645sUEBpwID9TblsSXBmTozNsMVFF4tC67jfn7xU130_provenance
{
dgn-np:NP403905.RAA9x645sUEBpwID9TblsSXBmTozNsMVFF4tC67jfn7xU130_assertion
dcterms:description
"[The genetic defect of familial combined hyperlipidemia (FCHL) is still unknown although FCHL is speculated to be the most prevalent genetic hyperlipidemia, and further investigations should be performed to elucidate the molecular mechanisms of FCHL]. 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:15256764
;
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:NP403905.RAA9x645sUEBpwID9TblsSXBmTozNsMVFF4tC67jfn7xU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:00+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" .
}