@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP658884.RA9kZadXgUxXYhPEYs1AHrD3YzvvPZPRUpfx7lepHclsU
> .
@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:NP658884.RA9kZadXgUxXYhPEYs1AHrD3YzvvPZPRUpfx7lepHclsU130_head
{
this:
np:hasAssertion
dgn-np:NP658884.RA9kZadXgUxXYhPEYs1AHrD3YzvvPZPRUpfx7lepHclsU130_assertion
;
np:hasProvenance
dgn-np:NP658884.RA9kZadXgUxXYhPEYs1AHrD3YzvvPZPRUpfx7lepHclsU130_provenance
;
np:hasPublicationInfo
dgn-np:NP658884.RA9kZadXgUxXYhPEYs1AHrD3YzvvPZPRUpfx7lepHclsU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP658884.RA9kZadXgUxXYhPEYs1AHrD3YzvvPZPRUpfx7lepHclsU130_assertion
a
np:Assertion
.
dgn-np:NP658884.RA9kZadXgUxXYhPEYs1AHrD3YzvvPZPRUpfx7lepHclsU130_provenance
a
np:Provenance
.
dgn-np:NP658884.RA9kZadXgUxXYhPEYs1AHrD3YzvvPZPRUpfx7lepHclsU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP658884.RA9kZadXgUxXYhPEYs1AHrD3YzvvPZPRUpfx7lepHclsU130_assertion
{
miriam-gene:80781
a
ncit:C16612
.
lld:C0020636
a
ncit:C7057
.
dgn-gda:DGN8c76540552321d350459a46effa4c503
sio:SIO_000628
miriam-gene:80781
,
lld:C0020636
;
a
sio:SIO_001121
.
}
dgn-np:NP658884.RA9kZadXgUxXYhPEYs1AHrD3YzvvPZPRUpfx7lepHclsU130_provenance
{
dgn-np:NP658884.RA9kZadXgUxXYhPEYs1AHrD3YzvvPZPRUpfx7lepHclsU130_assertion
dcterms:description
"[Endostatin deficiency may result in reduced or delayed regression of fetal blood vessels in the eye (including the intravitreal compartment), thereby resulting in incomplete development of the normal vasculature in the retina.]. 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:15465551
;
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:NP658884.RA9kZadXgUxXYhPEYs1AHrD3YzvvPZPRUpfx7lepHclsU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:38+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" .
}