@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP839951.RAgTfhgGkaNSNvIljxYKaV1b-F5eHetEeKvlRTANci2Cw
> .
@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/v3.0.0/void/
> .
dgn-np:NP839951.RAgTfhgGkaNSNvIljxYKaV1b-F5eHetEeKvlRTANci2Cw130_head
{
this:
np:hasAssertion
dgn-np:NP839951.RAgTfhgGkaNSNvIljxYKaV1b-F5eHetEeKvlRTANci2Cw130_assertion
;
np:hasProvenance
dgn-np:NP839951.RAgTfhgGkaNSNvIljxYKaV1b-F5eHetEeKvlRTANci2Cw130_provenance
;
np:hasPublicationInfo
dgn-np:NP839951.RAgTfhgGkaNSNvIljxYKaV1b-F5eHetEeKvlRTANci2Cw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP839951.RAgTfhgGkaNSNvIljxYKaV1b-F5eHetEeKvlRTANci2Cw130_assertion
a
np:Assertion
.
dgn-np:NP839951.RAgTfhgGkaNSNvIljxYKaV1b-F5eHetEeKvlRTANci2Cw130_provenance
a
np:Provenance
.
dgn-np:NP839951.RAgTfhgGkaNSNvIljxYKaV1b-F5eHetEeKvlRTANci2Cw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP839951.RAgTfhgGkaNSNvIljxYKaV1b-F5eHetEeKvlRTANci2Cw130_assertion
{
miriam-gene:10269
a
ncit:C16612
.
lld:C0004153
a
ncit:C7057
.
dgn-gda:DGN74c55e18c571397e3ae8542d11d3a392
sio:SIO_000628
miriam-gene:10269
,
lld:C0004153
;
a
sio:SIO_001121
.
}
dgn-np:NP839951.RAgTfhgGkaNSNvIljxYKaV1b-F5eHetEeKvlRTANci2Cw130_provenance
{
dgn-np:NP839951.RAgTfhgGkaNSNvIljxYKaV1b-F5eHetEeKvlRTANci2Cw130_assertion
dcterms:description
"[Although some common polymorphisms of LMNA have been associated with traits related to atherosclerosis, the monogenic diseases FPLD2 and HGPS are more likely to provide clues about new pathways for the general process of atherosclerosis.]. 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:15205220
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP839951.RAgTfhgGkaNSNvIljxYKaV1b-F5eHetEeKvlRTANci2Cw130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:46:10+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: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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}