@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP485864.RAOz-tl5Rn4hX9uAE4o0vNounLL_YqQKwXD-KVyOgQlk4
> .
@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:NP485864.RAOz-tl5Rn4hX9uAE4o0vNounLL_YqQKwXD-KVyOgQlk4130_head
{
this:
np:hasAssertion
dgn-np:NP485864.RAOz-tl5Rn4hX9uAE4o0vNounLL_YqQKwXD-KVyOgQlk4130_assertion
;
np:hasProvenance
dgn-np:NP485864.RAOz-tl5Rn4hX9uAE4o0vNounLL_YqQKwXD-KVyOgQlk4130_provenance
;
np:hasPublicationInfo
dgn-np:NP485864.RAOz-tl5Rn4hX9uAE4o0vNounLL_YqQKwXD-KVyOgQlk4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP485864.RAOz-tl5Rn4hX9uAE4o0vNounLL_YqQKwXD-KVyOgQlk4130_assertion
a
np:Assertion
.
dgn-np:NP485864.RAOz-tl5Rn4hX9uAE4o0vNounLL_YqQKwXD-KVyOgQlk4130_provenance
a
np:Provenance
.
dgn-np:NP485864.RAOz-tl5Rn4hX9uAE4o0vNounLL_YqQKwXD-KVyOgQlk4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP485864.RAOz-tl5Rn4hX9uAE4o0vNounLL_YqQKwXD-KVyOgQlk4130_assertion
{
miriam-gene:4000
a
ncit:C16612
.
lld:C0004153
a
ncit:C7057
.
dgn-gda:DGN98d0b5bb94f147a080499ae2628e01c3
sio:SIO_000628
miriam-gene:4000
,
lld:C0004153
;
a
sio:SIO_001121
.
}
dgn-np:NP485864.RAOz-tl5Rn4hX9uAE4o0vNounLL_YqQKwXD-KVyOgQlk4130_provenance
{
dgn-np:NP485864.RAOz-tl5Rn4hX9uAE4o0vNounLL_YqQKwXD-KVyOgQlk4130_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-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:NP485864.RAOz-tl5Rn4hX9uAE4o0vNounLL_YqQKwXD-KVyOgQlk4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:50+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" .
}