@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP228084.RAsqBqgxeoMsWYPmnKiXlw3PpdMyov5tRZAhd2omssEuY
> .
@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:NP228084.RAsqBqgxeoMsWYPmnKiXlw3PpdMyov5tRZAhd2omssEuY130_head
{
this:
np:hasAssertion
dgn-np:NP228084.RAsqBqgxeoMsWYPmnKiXlw3PpdMyov5tRZAhd2omssEuY130_assertion
;
np:hasProvenance
dgn-np:NP228084.RAsqBqgxeoMsWYPmnKiXlw3PpdMyov5tRZAhd2omssEuY130_provenance
;
np:hasPublicationInfo
dgn-np:NP228084.RAsqBqgxeoMsWYPmnKiXlw3PpdMyov5tRZAhd2omssEuY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP228084.RAsqBqgxeoMsWYPmnKiXlw3PpdMyov5tRZAhd2omssEuY130_assertion
a
np:Assertion
.
dgn-np:NP228084.RAsqBqgxeoMsWYPmnKiXlw3PpdMyov5tRZAhd2omssEuY130_provenance
a
np:Provenance
.
dgn-np:NP228084.RAsqBqgxeoMsWYPmnKiXlw3PpdMyov5tRZAhd2omssEuY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP228084.RAsqBqgxeoMsWYPmnKiXlw3PpdMyov5tRZAhd2omssEuY130_assertion
{
miriam-gene:6696
a
ncit:C16612
.
lld:C2939420
a
ncit:C7057
.
dgn-gda:DGN10ffcc118c5c7494901010e871e1c54b
sio:SIO_000628
miriam-gene:6696
,
lld:C2939420
;
a
sio:SIO_001121
.
}
dgn-np:NP228084.RAsqBqgxeoMsWYPmnKiXlw3PpdMyov5tRZAhd2omssEuY130_provenance
{
dgn-np:NP228084.RAsqBqgxeoMsWYPmnKiXlw3PpdMyov5tRZAhd2omssEuY130_assertion
dcterms:description
"[The expression patterns and functional roles of three osteopontin splice variants (OPNa, b, and c) in cancer metastasis and progression are not well understood due to the lack of reliable assays to differentiate the isoforms.]. 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:22188260
;
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:NP228084.RAsqBqgxeoMsWYPmnKiXlw3PpdMyov5tRZAhd2omssEuY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:08+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" .
}