@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP918094.RArETxmpEOaNk31WTx1jtSfPk9EANFQoPrb4nmPiyNE8k
> .
@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:NP918094.RArETxmpEOaNk31WTx1jtSfPk9EANFQoPrb4nmPiyNE8k130_head
{
this:
np:hasAssertion
dgn-np:NP918094.RArETxmpEOaNk31WTx1jtSfPk9EANFQoPrb4nmPiyNE8k130_assertion
;
np:hasProvenance
dgn-np:NP918094.RArETxmpEOaNk31WTx1jtSfPk9EANFQoPrb4nmPiyNE8k130_provenance
;
np:hasPublicationInfo
dgn-np:NP918094.RArETxmpEOaNk31WTx1jtSfPk9EANFQoPrb4nmPiyNE8k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP918094.RArETxmpEOaNk31WTx1jtSfPk9EANFQoPrb4nmPiyNE8k130_assertion
a
np:Assertion
.
dgn-np:NP918094.RArETxmpEOaNk31WTx1jtSfPk9EANFQoPrb4nmPiyNE8k130_provenance
a
np:Provenance
.
dgn-np:NP918094.RArETxmpEOaNk31WTx1jtSfPk9EANFQoPrb4nmPiyNE8k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP918094.RArETxmpEOaNk31WTx1jtSfPk9EANFQoPrb4nmPiyNE8k130_assertion
{
miriam-gene:55743
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGN1c2b2f0c9c76e1d82273910e657ecb59
sio:SIO_000628
miriam-gene:55743
,
lld:C0006142
;
a
sio:SIO_001121
.
}
dgn-np:NP918094.RArETxmpEOaNk31WTx1jtSfPk9EANFQoPrb4nmPiyNE8k130_provenance
{
dgn-np:NP918094.RArETxmpEOaNk31WTx1jtSfPk9EANFQoPrb4nmPiyNE8k130_assertion
dcterms:description
"[Notably, decreased CHFR expression resulted in the acquisition of many phenotypes associated with malignant progression, including accelerated growth rates, higher mitotic index, enhanced invasiveness, increased motility, greater aneuploidy, and amplified colony formation in soft agar, further supporting the role of CHFR as a tumor suppressor in breast cancer.]. 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:17596595
;
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:NP918094.RArETxmpEOaNk31WTx1jtSfPk9EANFQoPrb4nmPiyNE8k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:23+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" .
}