@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP265072.RAev81-bFP_x4U_2umG9QBYTyaSykslkXBCkPU-sJ1l8c
> .
@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:NP265072.RAev81-bFP_x4U_2umG9QBYTyaSykslkXBCkPU-sJ1l8c130_head
{
this:
np:hasAssertion
dgn-np:NP265072.RAev81-bFP_x4U_2umG9QBYTyaSykslkXBCkPU-sJ1l8c130_assertion
;
np:hasProvenance
dgn-np:NP265072.RAev81-bFP_x4U_2umG9QBYTyaSykslkXBCkPU-sJ1l8c130_provenance
;
np:hasPublicationInfo
dgn-np:NP265072.RAev81-bFP_x4U_2umG9QBYTyaSykslkXBCkPU-sJ1l8c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP265072.RAev81-bFP_x4U_2umG9QBYTyaSykslkXBCkPU-sJ1l8c130_assertion
a
np:Assertion
.
dgn-np:NP265072.RAev81-bFP_x4U_2umG9QBYTyaSykslkXBCkPU-sJ1l8c130_provenance
a
np:Provenance
.
dgn-np:NP265072.RAev81-bFP_x4U_2umG9QBYTyaSykslkXBCkPU-sJ1l8c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP265072.RAev81-bFP_x4U_2umG9QBYTyaSykslkXBCkPU-sJ1l8c130_assertion
{
miriam-gene:3576
a
ncit:C16612
.
lld:C0678222
a
ncit:C7057
.
dgn-gda:DGNfa9039527735f8c5f858a2b2ee1ae9c5
sio:SIO_000628
miriam-gene:3576
,
lld:C0678222
;
a
sio:SIO_001121
.
}
dgn-np:NP265072.RAev81-bFP_x4U_2umG9QBYTyaSykslkXBCkPU-sJ1l8c130_provenance
{
dgn-np:NP265072.RAev81-bFP_x4U_2umG9QBYTyaSykslkXBCkPU-sJ1l8c130_assertion
dcterms:description
"[In summary, i) routine quantitative DNA methylation assessment in NAF and MD samples is possible, and ii) genes hypermethylated in malignant breast tissue are also altered in matched NAF and in MD samples, and may be useful to assist in early breast cancer detection.]. 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:19618401
;
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:NP265072.RAev81-bFP_x4U_2umG9QBYTyaSykslkXBCkPU-sJ1l8c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:28+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" .
}