@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP795116.RAdjy8o-UzLVWXm2bJfKTgiKEwCo404ciciNr_JUX4ols
> .
@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:NP795116.RAdjy8o-UzLVWXm2bJfKTgiKEwCo404ciciNr_JUX4ols130_head
{
this:
np:hasAssertion
dgn-np:NP795116.RAdjy8o-UzLVWXm2bJfKTgiKEwCo404ciciNr_JUX4ols130_assertion
;
np:hasProvenance
dgn-np:NP795116.RAdjy8o-UzLVWXm2bJfKTgiKEwCo404ciciNr_JUX4ols130_provenance
;
np:hasPublicationInfo
dgn-np:NP795116.RAdjy8o-UzLVWXm2bJfKTgiKEwCo404ciciNr_JUX4ols130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP795116.RAdjy8o-UzLVWXm2bJfKTgiKEwCo404ciciNr_JUX4ols130_assertion
a
np:Assertion
.
dgn-np:NP795116.RAdjy8o-UzLVWXm2bJfKTgiKEwCo404ciciNr_JUX4ols130_provenance
a
np:Provenance
.
dgn-np:NP795116.RAdjy8o-UzLVWXm2bJfKTgiKEwCo404ciciNr_JUX4ols130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP795116.RAdjy8o-UzLVWXm2bJfKTgiKEwCo404ciciNr_JUX4ols130_assertion
{
miriam-gene:146
a
ncit:C16612
.
lld:C0268338
a
ncit:C7057
.
dgn-gda:DGNb22079c6ae6faf959b5cd543d5071e93
sio:SIO_000628
miriam-gene:146
,
lld:C0268338
;
a
sio:SIO_001121
.
}
dgn-np:NP795116.RAdjy8o-UzLVWXm2bJfKTgiKEwCo404ciciNr_JUX4ols130_provenance
{
dgn-np:NP795116.RAdjy8o-UzLVWXm2bJfKTgiKEwCo404ciciNr_JUX4ols130_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:NP795116.RAdjy8o-UzLVWXm2bJfKTgiKEwCo404ciciNr_JUX4ols130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:08+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" .
}