@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP833322.RAxLsT8o-6KhyTD8PKgjBm7lRk36-cX9rfSuL3VmbK5po
> .
@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:NP833322.RAxLsT8o-6KhyTD8PKgjBm7lRk36-cX9rfSuL3VmbK5po130_head
{
this:
np:hasAssertion
dgn-np:NP833322.RAxLsT8o-6KhyTD8PKgjBm7lRk36-cX9rfSuL3VmbK5po130_assertion
;
np:hasProvenance
dgn-np:NP833322.RAxLsT8o-6KhyTD8PKgjBm7lRk36-cX9rfSuL3VmbK5po130_provenance
;
np:hasPublicationInfo
dgn-np:NP833322.RAxLsT8o-6KhyTD8PKgjBm7lRk36-cX9rfSuL3VmbK5po130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP833322.RAxLsT8o-6KhyTD8PKgjBm7lRk36-cX9rfSuL3VmbK5po130_assertion
a
np:Assertion
.
dgn-np:NP833322.RAxLsT8o-6KhyTD8PKgjBm7lRk36-cX9rfSuL3VmbK5po130_provenance
a
np:Provenance
.
dgn-np:NP833322.RAxLsT8o-6KhyTD8PKgjBm7lRk36-cX9rfSuL3VmbK5po130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP833322.RAxLsT8o-6KhyTD8PKgjBm7lRk36-cX9rfSuL3VmbK5po130_assertion
{
miriam-gene:4318
a
ncit:C16612
.
lld:C1520166
a
ncit:C7057
.
dgn-gda:DGNc84649c678f596bf49da8a30b5e3e36a
sio:SIO_000628
miriam-gene:4318
,
lld:C1520166
;
a
sio:SIO_001121
.
}
dgn-np:NP833322.RAxLsT8o-6KhyTD8PKgjBm7lRk36-cX9rfSuL3VmbK5po130_provenance
{
dgn-np:NP833322.RAxLsT8o-6KhyTD8PKgjBm7lRk36-cX9rfSuL3VmbK5po130_assertion
dcterms:description
"[MMP-9 silencing cells with short hairpin RNA dramatically blocked the cellular infiltrative pattern, hypervascularity, and cell proliferation in vivo, and decreased cell invasion, colony formation, and cell motility in vitro, indicating that a high level of MMP-9 plays an essential role in extensive infiltration and hypervascularity in the xenograft model.]. 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:20413683
;
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:NP833322.RAxLsT8o-6KhyTD8PKgjBm7lRk36-cX9rfSuL3VmbK5po130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:30+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" .
}