@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP484957.RAxtSwBzwXfPn9PBQ2jCQMHAukOKYRr5bRSIpkX-5pT6s
> .
@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:NP484957.RAxtSwBzwXfPn9PBQ2jCQMHAukOKYRr5bRSIpkX-5pT6s130_head
{
this:
np:hasAssertion
dgn-np:NP484957.RAxtSwBzwXfPn9PBQ2jCQMHAukOKYRr5bRSIpkX-5pT6s130_assertion
;
np:hasProvenance
dgn-np:NP484957.RAxtSwBzwXfPn9PBQ2jCQMHAukOKYRr5bRSIpkX-5pT6s130_provenance
;
np:hasPublicationInfo
dgn-np:NP484957.RAxtSwBzwXfPn9PBQ2jCQMHAukOKYRr5bRSIpkX-5pT6s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP484957.RAxtSwBzwXfPn9PBQ2jCQMHAukOKYRr5bRSIpkX-5pT6s130_assertion
a
np:Assertion
.
dgn-np:NP484957.RAxtSwBzwXfPn9PBQ2jCQMHAukOKYRr5bRSIpkX-5pT6s130_provenance
a
np:Provenance
.
dgn-np:NP484957.RAxtSwBzwXfPn9PBQ2jCQMHAukOKYRr5bRSIpkX-5pT6s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP484957.RAxtSwBzwXfPn9PBQ2jCQMHAukOKYRr5bRSIpkX-5pT6s130_assertion
{
miriam-gene:2006
a
ncit:C16612
.
lld:C0007766
a
ncit:C7057
.
dgn-gda:DGNee87dfb31b5f09948ec2706acea6fddd
sio:SIO_000628
miriam-gene:2006
,
lld:C0007766
;
a
sio:SIO_001121
.
}
dgn-np:NP484957.RAxtSwBzwXfPn9PBQ2jCQMHAukOKYRr5bRSIpkX-5pT6s130_provenance
{
dgn-np:NP484957.RAxtSwBzwXfPn9PBQ2jCQMHAukOKYRr5bRSIpkX-5pT6s130_assertion
dcterms:description
"[Lysyl oxidase is a promising candidate gene for a mutation search in intracranial aneurysm families because (a) it controls the processing, cross-linking and maturation of collagen and elastin fibers in the blood vessel wall, (b) its expression levels and activity are altered in different animal models of aneurysm pathogenesis, and (c) it is encoded within the chromosome 5q22-31 region of suggestive linkage to intracranial aneurysms.]. 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:15273433
;
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:NP484957.RAxtSwBzwXfPn9PBQ2jCQMHAukOKYRr5bRSIpkX-5pT6s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:50+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" .
}