@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP443388.RAEnjRwUeiaQmxkFjWHhUyN6si7yn_YYH95qfG_o2a_Iw
> .
@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:NP443388.RAEnjRwUeiaQmxkFjWHhUyN6si7yn_YYH95qfG_o2a_Iw130_head
{
this:
np:hasAssertion
dgn-np:NP443388.RAEnjRwUeiaQmxkFjWHhUyN6si7yn_YYH95qfG_o2a_Iw130_assertion
;
np:hasProvenance
dgn-np:NP443388.RAEnjRwUeiaQmxkFjWHhUyN6si7yn_YYH95qfG_o2a_Iw130_provenance
;
np:hasPublicationInfo
dgn-np:NP443388.RAEnjRwUeiaQmxkFjWHhUyN6si7yn_YYH95qfG_o2a_Iw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP443388.RAEnjRwUeiaQmxkFjWHhUyN6si7yn_YYH95qfG_o2a_Iw130_assertion
a
np:Assertion
.
dgn-np:NP443388.RAEnjRwUeiaQmxkFjWHhUyN6si7yn_YYH95qfG_o2a_Iw130_provenance
a
np:Provenance
.
dgn-np:NP443388.RAEnjRwUeiaQmxkFjWHhUyN6si7yn_YYH95qfG_o2a_Iw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP443388.RAEnjRwUeiaQmxkFjWHhUyN6si7yn_YYH95qfG_o2a_Iw130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0178874
a
ncit:C7057
.
dgn-gda:DGNb0afa1d6a76ff3911f404d78a6591a4e
sio:SIO_000628
miriam-gene:3342
,
lld:C0178874
;
a
sio:SIO_001121
.
}
dgn-np:NP443388.RAEnjRwUeiaQmxkFjWHhUyN6si7yn_YYH95qfG_o2a_Iw130_provenance
{
dgn-np:NP443388.RAEnjRwUeiaQmxkFjWHhUyN6si7yn_YYH95qfG_o2a_Iw130_assertion
dcterms:description
"[The low frequency of aberrations detectable by CGH in overtly malignant myoepithelial neoplasms suggests that gross cytogenetic alterations were acquired in the course of tumour progression and points to the relevance of genetic changes not resolved by CGH.]. 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:12434418
;
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:NP443388.RAEnjRwUeiaQmxkFjWHhUyN6si7yn_YYH95qfG_o2a_Iw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:24+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" .
}