@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP162102.RAAFoQ4A51ydAkwGdeaEwkqFYEWUmQcf70KC9Ds61-PCE
> .
@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:NP162102.RAAFoQ4A51ydAkwGdeaEwkqFYEWUmQcf70KC9Ds61-PCE130_head
{
this:
np:hasAssertion
dgn-np:NP162102.RAAFoQ4A51ydAkwGdeaEwkqFYEWUmQcf70KC9Ds61-PCE130_assertion
;
np:hasProvenance
dgn-np:NP162102.RAAFoQ4A51ydAkwGdeaEwkqFYEWUmQcf70KC9Ds61-PCE130_provenance
;
np:hasPublicationInfo
dgn-np:NP162102.RAAFoQ4A51ydAkwGdeaEwkqFYEWUmQcf70KC9Ds61-PCE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP162102.RAAFoQ4A51ydAkwGdeaEwkqFYEWUmQcf70KC9Ds61-PCE130_assertion
a
np:Assertion
.
dgn-np:NP162102.RAAFoQ4A51ydAkwGdeaEwkqFYEWUmQcf70KC9Ds61-PCE130_provenance
a
np:Provenance
.
dgn-np:NP162102.RAAFoQ4A51ydAkwGdeaEwkqFYEWUmQcf70KC9Ds61-PCE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP162102.RAAFoQ4A51ydAkwGdeaEwkqFYEWUmQcf70KC9Ds61-PCE130_assertion
{
miriam-gene:1588
a
ncit:C16612
.
lld:C0678222
a
ncit:C7057
.
dgn-gda:DGN3f69fffe7280f60ef4f66a29c745c867
sio:SIO_000628
miriam-gene:1588
,
lld:C0678222
;
a
sio:SIO_001121
.
}
dgn-np:NP162102.RAAFoQ4A51ydAkwGdeaEwkqFYEWUmQcf70KC9Ds61-PCE130_provenance
{
dgn-np:NP162102.RAAFoQ4A51ydAkwGdeaEwkqFYEWUmQcf70KC9Ds61-PCE130_assertion
dcterms:description
"[Hence, further efforts aimed to study the contribution of genetic mutations in other genes, including the estrogen receptor gene, TP53, CYP19, and mismatch repair genes to further investigate the genetic component of 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:21875255
;
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:NP162102.RAAFoQ4A51ydAkwGdeaEwkqFYEWUmQcf70KC9Ds61-PCE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:27+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" .
}