@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP883591.RA0LyrGWh1urQj2xeF6Ggo7uLbgqDZW0IRBtnH9BICibU
> .
@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:NP883591.RA0LyrGWh1urQj2xeF6Ggo7uLbgqDZW0IRBtnH9BICibU130_head
{
this:
np:hasAssertion
dgn-np:NP883591.RA0LyrGWh1urQj2xeF6Ggo7uLbgqDZW0IRBtnH9BICibU130_assertion
;
np:hasProvenance
dgn-np:NP883591.RA0LyrGWh1urQj2xeF6Ggo7uLbgqDZW0IRBtnH9BICibU130_provenance
;
np:hasPublicationInfo
dgn-np:NP883591.RA0LyrGWh1urQj2xeF6Ggo7uLbgqDZW0IRBtnH9BICibU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP883591.RA0LyrGWh1urQj2xeF6Ggo7uLbgqDZW0IRBtnH9BICibU130_assertion
a
np:Assertion
.
dgn-np:NP883591.RA0LyrGWh1urQj2xeF6Ggo7uLbgqDZW0IRBtnH9BICibU130_provenance
a
np:Provenance
.
dgn-np:NP883591.RA0LyrGWh1urQj2xeF6Ggo7uLbgqDZW0IRBtnH9BICibU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP883591.RA0LyrGWh1urQj2xeF6Ggo7uLbgqDZW0IRBtnH9BICibU130_assertion
{
miriam-gene:771
a
ncit:C16612
.
lld:C1458156
a
ncit:C7057
.
dgn-gda:DGNa7d1369ced91b11e00418cf7cc3549ae
sio:SIO_000628
miriam-gene:771
,
lld:C1458156
;
a
sio:SIO_001121
.
}
dgn-np:NP883591.RA0LyrGWh1urQj2xeF6Ggo7uLbgqDZW0IRBtnH9BICibU130_provenance
{
dgn-np:NP883591.RA0LyrGWh1urQj2xeF6Ggo7uLbgqDZW0IRBtnH9BICibU130_assertion
dcterms:description
"[In the initial validation of the seven putative markers of metastatic LN, the Cox proportional hazard model pointed to SFN, CA12 and JUP expression to significantly relate to the time to groin recurrence in VC patients.]. 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:22673103
;
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:NP883591.RA0LyrGWh1urQj2xeF6Ggo7uLbgqDZW0IRBtnH9BICibU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:59+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" .
}