@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP347808.RA1N-iDXy26DYKDZuTOLpF_AlO1hZeKf9i7JjUfEVfRgE
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP347808.RA1N-iDXy26DYKDZuTOLpF_AlO1hZeKf9i7JjUfEVfRgE130_assertion
;
np:hasProvenance
dgn-np:NP347808.RA1N-iDXy26DYKDZuTOLpF_AlO1hZeKf9i7JjUfEVfRgE130_provenance
;
np:hasPublicationInfo
dgn-np:NP347808.RA1N-iDXy26DYKDZuTOLpF_AlO1hZeKf9i7JjUfEVfRgE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP347808.RA1N-iDXy26DYKDZuTOLpF_AlO1hZeKf9i7JjUfEVfRgE130_assertion
a
np:Assertion
.
dgn-np:NP347808.RA1N-iDXy26DYKDZuTOLpF_AlO1hZeKf9i7JjUfEVfRgE130_provenance
a
np:Provenance
.
dgn-np:NP347808.RA1N-iDXy26DYKDZuTOLpF_AlO1hZeKf9i7JjUfEVfRgE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP347808.RA1N-iDXy26DYKDZuTOLpF_AlO1hZeKf9i7JjUfEVfRgE130_assertion
{
miriam-gene:11235
a
ncit:C16612
.
lld:C2919945
a
ncit:C7057
.
dgn-gda:DGN8c77bf06472f73198a78434028ae7829
sio:SIO_000628
miriam-gene:11235
,
lld:C2919945
;
a
sio:SIO_001121
.
}
dgn-np:NP347808.RA1N-iDXy26DYKDZuTOLpF_AlO1hZeKf9i7JjUfEVfRgE130_provenance
{
dgn-np:NP347808.RA1N-iDXy26DYKDZuTOLpF_AlO1hZeKf9i7JjUfEVfRgE130_assertion
dcterms:description
"[This article summarizes the recent cloning of the CCM1, CCM2, and CCM3 genes, which are responsible for autosomal dominant CCM, and also describes current hypotheses for their roles in integrin and p38 mitogen-activated protein kinase- mediated regulation of angiogenesis.]. 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:16131422
;
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:NP347808.RA1N-iDXy26DYKDZuTOLpF_AlO1hZeKf9i7JjUfEVfRgE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:24+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" .
}