@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP394159.RAvNTOeSjGXfst28WUkGniWL2ijH4pL_g7N5eS3VK-ovI
> .
@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:NP394159.RAvNTOeSjGXfst28WUkGniWL2ijH4pL_g7N5eS3VK-ovI130_head
{
this:
np:hasAssertion
dgn-np:NP394159.RAvNTOeSjGXfst28WUkGniWL2ijH4pL_g7N5eS3VK-ovI130_assertion
;
np:hasProvenance
dgn-np:NP394159.RAvNTOeSjGXfst28WUkGniWL2ijH4pL_g7N5eS3VK-ovI130_provenance
;
np:hasPublicationInfo
dgn-np:NP394159.RAvNTOeSjGXfst28WUkGniWL2ijH4pL_g7N5eS3VK-ovI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP394159.RAvNTOeSjGXfst28WUkGniWL2ijH4pL_g7N5eS3VK-ovI130_assertion
a
np:Assertion
.
dgn-np:NP394159.RAvNTOeSjGXfst28WUkGniWL2ijH4pL_g7N5eS3VK-ovI130_provenance
a
np:Provenance
.
dgn-np:NP394159.RAvNTOeSjGXfst28WUkGniWL2ijH4pL_g7N5eS3VK-ovI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP394159.RAvNTOeSjGXfst28WUkGniWL2ijH4pL_g7N5eS3VK-ovI130_assertion
{
miriam-gene:4085
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGN48bbd79bc9d79206b9dacceb67871f83
sio:SIO_000628
miriam-gene:4085
,
lld:C0006142
;
a
sio:SIO_001121
.
}
dgn-np:NP394159.RAvNTOeSjGXfst28WUkGniWL2ijH4pL_g7N5eS3VK-ovI130_provenance
{
dgn-np:NP394159.RAvNTOeSjGXfst28WUkGniWL2ijH4pL_g7N5eS3VK-ovI130_assertion
dcterms:description
"[To explore further the potential role of MAD2L1 in breast cancer, we analyzed MAD2L1 gene expression in 13 minimally to grossly aneuploid human breast cancer cell lines and found significant differences of expression in three lines.]. 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:11066082
;
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:NP394159.RAvNTOeSjGXfst28WUkGniWL2ijH4pL_g7N5eS3VK-ovI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:54+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" .
}