@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP719280.RACm6sIR0o_pDyFaTWm1yDIvjjpkQz7SCY9znnQ60X6WE
> .
@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:NP719280.RACm6sIR0o_pDyFaTWm1yDIvjjpkQz7SCY9znnQ60X6WE130_head
{
this:
np:hasAssertion
dgn-np:NP719280.RACm6sIR0o_pDyFaTWm1yDIvjjpkQz7SCY9znnQ60X6WE130_assertion
;
np:hasProvenance
dgn-np:NP719280.RACm6sIR0o_pDyFaTWm1yDIvjjpkQz7SCY9znnQ60X6WE130_provenance
;
np:hasPublicationInfo
dgn-np:NP719280.RACm6sIR0o_pDyFaTWm1yDIvjjpkQz7SCY9znnQ60X6WE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP719280.RACm6sIR0o_pDyFaTWm1yDIvjjpkQz7SCY9znnQ60X6WE130_assertion
a
np:Assertion
.
dgn-np:NP719280.RACm6sIR0o_pDyFaTWm1yDIvjjpkQz7SCY9znnQ60X6WE130_provenance
a
np:Provenance
.
dgn-np:NP719280.RACm6sIR0o_pDyFaTWm1yDIvjjpkQz7SCY9znnQ60X6WE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP719280.RACm6sIR0o_pDyFaTWm1yDIvjjpkQz7SCY9znnQ60X6WE130_assertion
{
miriam-gene:146
a
ncit:C16612
.
lld:C0340613
a
ncit:C7057
.
dgn-gda:DGNa558ab0707c2e5b9acf45276a1cb26a7
sio:SIO_000628
miriam-gene:146
,
lld:C0340613
;
a
sio:SIO_001121
.
}
dgn-np:NP719280.RACm6sIR0o_pDyFaTWm1yDIvjjpkQz7SCY9znnQ60X6WE130_provenance
{
dgn-np:NP719280.RACm6sIR0o_pDyFaTWm1yDIvjjpkQz7SCY9znnQ60X6WE130_assertion
dcterms:description
"[There is now strong evidence for the implication of collagen alpha 1(I), alpha 2(I) and alpha 1(III) mutations in many forms of osteogenesis imperfecta and inherited arterial aneurysms (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:2572730
;
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:NP719280.RACm6sIR0o_pDyFaTWm1yDIvjjpkQz7SCY9znnQ60X6WE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:17+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" .
}