@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP755217.RAuetVp83bYbtQVJYyDtT6Jv53ExHo7Nu0euWEnZEzSlc
> .
@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:NP755217.RAuetVp83bYbtQVJYyDtT6Jv53ExHo7Nu0euWEnZEzSlc130_head
{
this:
np:hasAssertion
dgn-np:NP755217.RAuetVp83bYbtQVJYyDtT6Jv53ExHo7Nu0euWEnZEzSlc130_assertion
;
np:hasProvenance
dgn-np:NP755217.RAuetVp83bYbtQVJYyDtT6Jv53ExHo7Nu0euWEnZEzSlc130_provenance
;
np:hasPublicationInfo
dgn-np:NP755217.RAuetVp83bYbtQVJYyDtT6Jv53ExHo7Nu0euWEnZEzSlc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP755217.RAuetVp83bYbtQVJYyDtT6Jv53ExHo7Nu0euWEnZEzSlc130_assertion
a
np:Assertion
.
dgn-np:NP755217.RAuetVp83bYbtQVJYyDtT6Jv53ExHo7Nu0euWEnZEzSlc130_provenance
a
np:Provenance
.
dgn-np:NP755217.RAuetVp83bYbtQVJYyDtT6Jv53ExHo7Nu0euWEnZEzSlc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP755217.RAuetVp83bYbtQVJYyDtT6Jv53ExHo7Nu0euWEnZEzSlc130_assertion
{
miriam-gene:2006
a
ncit:C16612
.
lld:C0024796
a
ncit:C7057
.
dgn-gda:DGN0a5c9039e48fffb99fc59393ec94dee3
sio:SIO_000628
miriam-gene:2006
,
lld:C0024796
;
a
sio:SIO_001121
.
}
dgn-np:NP755217.RAuetVp83bYbtQVJYyDtT6Jv53ExHo7Nu0euWEnZEzSlc130_provenance
{
dgn-np:NP755217.RAuetVp83bYbtQVJYyDtT6Jv53ExHo7Nu0euWEnZEzSlc130_assertion
dcterms:description
"[Although the underlying biochemical and molecular defect(s) of this pleiotropic disease is currently unknown, we have consistently observed apparent diminished content of elastin-associated microfibrillar fibers accumulating in skin, or produced by cultured fibroblasts, from patients with the Marfan syndrome and have documented the cosegregation of these immunofluorescent abnormalities of microfibrillar fibers with the Marfan syndrome phenotype in family studies.]. 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:2180285
;
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:NP755217.RAuetVp83bYbtQVJYyDtT6Jv53ExHo7Nu0euWEnZEzSlc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:37+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" .
}