@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP789053.RA5QxuRhbdCfjhfyOmPH7TM7axCtnvHxTtxsAfphkvijQ
> .
@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:NP789053.RA5QxuRhbdCfjhfyOmPH7TM7axCtnvHxTtxsAfphkvijQ130_head
{
this:
np:hasAssertion
dgn-np:NP789053.RA5QxuRhbdCfjhfyOmPH7TM7axCtnvHxTtxsAfphkvijQ130_assertion
;
np:hasProvenance
dgn-np:NP789053.RA5QxuRhbdCfjhfyOmPH7TM7axCtnvHxTtxsAfphkvijQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP789053.RA5QxuRhbdCfjhfyOmPH7TM7axCtnvHxTtxsAfphkvijQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP789053.RA5QxuRhbdCfjhfyOmPH7TM7axCtnvHxTtxsAfphkvijQ130_assertion
a
np:Assertion
.
dgn-np:NP789053.RA5QxuRhbdCfjhfyOmPH7TM7axCtnvHxTtxsAfphkvijQ130_provenance
a
np:Provenance
.
dgn-np:NP789053.RA5QxuRhbdCfjhfyOmPH7TM7axCtnvHxTtxsAfphkvijQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP789053.RA5QxuRhbdCfjhfyOmPH7TM7axCtnvHxTtxsAfphkvijQ130_assertion
{
miriam-gene:1281
a
ncit:C16612
.
lld:C0019247
a
ncit:C7057
.
dgn-gda:DGN96a4f2c0c4057f45ddaa0dde82dc2cf5
sio:SIO_000628
miriam-gene:1281
,
lld:C0019247
;
a
sio:SIO_001121
.
}
dgn-np:NP789053.RA5QxuRhbdCfjhfyOmPH7TM7axCtnvHxTtxsAfphkvijQ130_provenance
{
dgn-np:NP789053.RA5QxuRhbdCfjhfyOmPH7TM7axCtnvHxTtxsAfphkvijQ130_assertion
dcterms:description
"[Experiments were carried out to test the hypothesis that familial aortic aneurysms, either thoracic or abdominal, are caused by mutations in the gene for type III procollagen (COL3A1) similar to mutations in the same gene that have been shown to cause rupture of aorta and other disastrous consequences in the rare genetic disorder known as Ehlers-Danlos syndrome type IV.]. 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:2243125
;
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:NP789053.RA5QxuRhbdCfjhfyOmPH7TM7axCtnvHxTtxsAfphkvijQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:01+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" .
}