@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP422294.RAHtZWz-i4A3NbKc4yGOeRh3Gzno4C0-8TP_ZMdgP37-c
> .
@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:NP422294.RAHtZWz-i4A3NbKc4yGOeRh3Gzno4C0-8TP_ZMdgP37-c130_head
{
this:
np:hasAssertion
dgn-np:NP422294.RAHtZWz-i4A3NbKc4yGOeRh3Gzno4C0-8TP_ZMdgP37-c130_assertion
;
np:hasProvenance
dgn-np:NP422294.RAHtZWz-i4A3NbKc4yGOeRh3Gzno4C0-8TP_ZMdgP37-c130_provenance
;
np:hasPublicationInfo
dgn-np:NP422294.RAHtZWz-i4A3NbKc4yGOeRh3Gzno4C0-8TP_ZMdgP37-c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP422294.RAHtZWz-i4A3NbKc4yGOeRh3Gzno4C0-8TP_ZMdgP37-c130_assertion
a
np:Assertion
.
dgn-np:NP422294.RAHtZWz-i4A3NbKc4yGOeRh3Gzno4C0-8TP_ZMdgP37-c130_provenance
a
np:Provenance
.
dgn-np:NP422294.RAHtZWz-i4A3NbKc4yGOeRh3Gzno4C0-8TP_ZMdgP37-c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP422294.RAHtZWz-i4A3NbKc4yGOeRh3Gzno4C0-8TP_ZMdgP37-c130_assertion
{
miriam-gene:1281
a
ncit:C16612
.
lld:C0042143
a
ncit:C7057
.
dgn-gda:DGNf475bc28d80770f9e78e65887a177c87
sio:SIO_000628
miriam-gene:1281
,
lld:C0042143
;
a
sio:SIO_001121
.
}
dgn-np:NP422294.RAHtZWz-i4A3NbKc4yGOeRh3Gzno4C0-8TP_ZMdgP37-c130_provenance
{
dgn-np:NP422294.RAHtZWz-i4A3NbKc4yGOeRh3Gzno4C0-8TP_ZMdgP37-c130_assertion
dcterms:description
"[The vascular type of the Ehlers-Danlos syndrome (Ehlers-Danlos syndrome type IV, EDS IV; OMIM #130050) is a rare connective tissue disorder with autosomal dominant transmission caused by mutations in the COL3A1 gene resulting in increased fragility of connective tissue with arterial, intestinal, and uterine ruptures and premature death.]. 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:23489429
;
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:NP422294.RAHtZWz-i4A3NbKc4yGOeRh3Gzno4C0-8TP_ZMdgP37-c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:10+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: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" .
}