@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP371806.RA7ZTB99-NiFGIGa4GlSzRL3L_vOjQJd_tOt_o8V0QPKw
> .
@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:NP371806.RA7ZTB99-NiFGIGa4GlSzRL3L_vOjQJd_tOt_o8V0QPKw130_head
{
this:
np:hasAssertion
dgn-np:NP371806.RA7ZTB99-NiFGIGa4GlSzRL3L_vOjQJd_tOt_o8V0QPKw130_assertion
;
np:hasProvenance
dgn-np:NP371806.RA7ZTB99-NiFGIGa4GlSzRL3L_vOjQJd_tOt_o8V0QPKw130_provenance
;
np:hasPublicationInfo
dgn-np:NP371806.RA7ZTB99-NiFGIGa4GlSzRL3L_vOjQJd_tOt_o8V0QPKw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP371806.RA7ZTB99-NiFGIGa4GlSzRL3L_vOjQJd_tOt_o8V0QPKw130_assertion
a
np:Assertion
.
dgn-np:NP371806.RA7ZTB99-NiFGIGa4GlSzRL3L_vOjQJd_tOt_o8V0QPKw130_provenance
a
np:Provenance
.
dgn-np:NP371806.RA7ZTB99-NiFGIGa4GlSzRL3L_vOjQJd_tOt_o8V0QPKw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP371806.RA7ZTB99-NiFGIGa4GlSzRL3L_vOjQJd_tOt_o8V0QPKw130_assertion
{
miriam-gene:7428
a
ncit:C16612
.
lld:C0002940
a
ncit:C7057
.
dgn-gda:DGNe10fb10d2313b7f0378d17e9b13e82c6
sio:SIO_000628
miriam-gene:7428
,
lld:C0002940
;
a
sio:SIO_001121
.
}
dgn-np:NP371806.RA7ZTB99-NiFGIGa4GlSzRL3L_vOjQJd_tOt_o8V0QPKw130_provenance
{
dgn-np:NP371806.RA7ZTB99-NiFGIGa4GlSzRL3L_vOjQJd_tOt_o8V0QPKw130_assertion
dcterms:description
"[Although a single point mutation is unlikely to be responsible for the complex phenotype of intracranial aneurysm, further research on aneurysmal domes and VHL gene expression may help validate the theory that extracellular matrix destruction is the final common pathway to aneurysm formation.]. 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:16506495
;
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:NP371806.RA7ZTB99-NiFGIGa4GlSzRL3L_vOjQJd_tOt_o8V0QPKw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:38+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" .
}