@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP766806.RAFAYsGsaRt0PPkEAwGEPEjIpvyArb3QKDk2FfyYC4dPs
> .
@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:NP766806.RAFAYsGsaRt0PPkEAwGEPEjIpvyArb3QKDk2FfyYC4dPs130_head
{
this:
np:hasAssertion
dgn-np:NP766806.RAFAYsGsaRt0PPkEAwGEPEjIpvyArb3QKDk2FfyYC4dPs130_assertion
;
np:hasProvenance
dgn-np:NP766806.RAFAYsGsaRt0PPkEAwGEPEjIpvyArb3QKDk2FfyYC4dPs130_provenance
;
np:hasPublicationInfo
dgn-np:NP766806.RAFAYsGsaRt0PPkEAwGEPEjIpvyArb3QKDk2FfyYC4dPs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP766806.RAFAYsGsaRt0PPkEAwGEPEjIpvyArb3QKDk2FfyYC4dPs130_assertion
a
np:Assertion
.
dgn-np:NP766806.RAFAYsGsaRt0PPkEAwGEPEjIpvyArb3QKDk2FfyYC4dPs130_provenance
a
np:Provenance
.
dgn-np:NP766806.RAFAYsGsaRt0PPkEAwGEPEjIpvyArb3QKDk2FfyYC4dPs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP766806.RAFAYsGsaRt0PPkEAwGEPEjIpvyArb3QKDk2FfyYC4dPs130_assertion
{
miriam-gene:650
a
ncit:C16612
.
lld:C0600139
a
ncit:C7057
.
dgn-gda:DGN3cd6ea20e8c60face1d4f31136f4fc21
sio:SIO_000628
miriam-gene:650
,
lld:C0600139
;
a
sio:SIO_001121
.
}
dgn-np:NP766806.RAFAYsGsaRt0PPkEAwGEPEjIpvyArb3QKDk2FfyYC4dPs130_provenance
{
dgn-np:NP766806.RAFAYsGsaRt0PPkEAwGEPEjIpvyArb3QKDk2FfyYC4dPs130_assertion
dcterms:description
"[These data suggest that decreased BMP2, nuclear smad8 and nuclear Smad4 expression are associated with the progression to PC, and in particular loss of BMP2 and Smad4 are related to progression to a more aggressive phenotype.]. 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:15042598
;
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:NP766806.RAFAYsGsaRt0PPkEAwGEPEjIpvyArb3QKDk2FfyYC4dPs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:44+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" .
}