@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP260409.RApLmm1mXpqhRMtfyLknpAxkYK9WnS_i0ez6e9_M6w6rc
> .
@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:NP260409.RApLmm1mXpqhRMtfyLknpAxkYK9WnS_i0ez6e9_M6w6rc130_head
{
this:
np:hasAssertion
dgn-np:NP260409.RApLmm1mXpqhRMtfyLknpAxkYK9WnS_i0ez6e9_M6w6rc130_assertion
;
np:hasProvenance
dgn-np:NP260409.RApLmm1mXpqhRMtfyLknpAxkYK9WnS_i0ez6e9_M6w6rc130_provenance
;
np:hasPublicationInfo
dgn-np:NP260409.RApLmm1mXpqhRMtfyLknpAxkYK9WnS_i0ez6e9_M6w6rc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP260409.RApLmm1mXpqhRMtfyLknpAxkYK9WnS_i0ez6e9_M6w6rc130_assertion
a
np:Assertion
.
dgn-np:NP260409.RApLmm1mXpqhRMtfyLknpAxkYK9WnS_i0ez6e9_M6w6rc130_provenance
a
np:Provenance
.
dgn-np:NP260409.RApLmm1mXpqhRMtfyLknpAxkYK9WnS_i0ez6e9_M6w6rc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP260409.RApLmm1mXpqhRMtfyLknpAxkYK9WnS_i0ez6e9_M6w6rc130_assertion
{
miriam-gene:302
a
ncit:C16612
.
lld:C0011884
a
ncit:C7057
.
dgn-gda:DGN52b90c86fc3421e2339bb28480b6659b
sio:SIO_000628
miriam-gene:302
,
lld:C0011884
;
a
sio:SIO_001121
.
}
dgn-np:NP260409.RApLmm1mXpqhRMtfyLknpAxkYK9WnS_i0ez6e9_M6w6rc130_provenance
{
dgn-np:NP260409.RApLmm1mXpqhRMtfyLknpAxkYK9WnS_i0ez6e9_M6w6rc130_assertion
dcterms:description
"[This study supports the hypothesis that annexin A2 is an important target for treatment of neovascular diseases and suggests that TM601, through its interaction with annexin A2, causes suppression and regression of ocular NV and reduces vascular leakage and thus may provide a new treatment for blinding diseases such as neovascular age-related macular degeneration and diabetic retinopathy.]. 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:20607799
;
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:NP260409.RApLmm1mXpqhRMtfyLknpAxkYK9WnS_i0ez6e9_M6w6rc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:25+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" .
}