@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP170961.RAPyUqbnIz8KNT6jqFptvf9Pioom_BX1GAJWcpKRp5hJI
> .
@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:NP170961.RAPyUqbnIz8KNT6jqFptvf9Pioom_BX1GAJWcpKRp5hJI130_head
{
this:
np:hasAssertion
dgn-np:NP170961.RAPyUqbnIz8KNT6jqFptvf9Pioom_BX1GAJWcpKRp5hJI130_assertion
;
np:hasProvenance
dgn-np:NP170961.RAPyUqbnIz8KNT6jqFptvf9Pioom_BX1GAJWcpKRp5hJI130_provenance
;
np:hasPublicationInfo
dgn-np:NP170961.RAPyUqbnIz8KNT6jqFptvf9Pioom_BX1GAJWcpKRp5hJI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP170961.RAPyUqbnIz8KNT6jqFptvf9Pioom_BX1GAJWcpKRp5hJI130_assertion
a
np:Assertion
.
dgn-np:NP170961.RAPyUqbnIz8KNT6jqFptvf9Pioom_BX1GAJWcpKRp5hJI130_provenance
a
np:Provenance
.
dgn-np:NP170961.RAPyUqbnIz8KNT6jqFptvf9Pioom_BX1GAJWcpKRp5hJI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP170961.RAPyUqbnIz8KNT6jqFptvf9Pioom_BX1GAJWcpKRp5hJI130_assertion
{
miriam-gene:7422
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGN986b596fb59e7050d405df3dd365cfb2
sio:SIO_000628
miriam-gene:7422
,
lld:C0006142
;
a
sio:SIO_001121
.
}
dgn-np:NP170961.RAPyUqbnIz8KNT6jqFptvf9Pioom_BX1GAJWcpKRp5hJI130_provenance
{
dgn-np:NP170961.RAPyUqbnIz8KNT6jqFptvf9Pioom_BX1GAJWcpKRp5hJI130_assertion
dcterms:description
"[The wild and the variant alleles of the C936T and G634C vascular endothelial grow factor (VEGF) polymorphisms seem to be linked to higher angiogenic phenotype than the remaining alleles and may act on breast cancer (BC) origin.]. 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:20981515
;
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:NP170961.RAPyUqbnIz8KNT6jqFptvf9Pioom_BX1GAJWcpKRp5hJI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:32+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" .
}