@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP155886.RASbdFa8GZHQtkdD6DKTFYLX8_WMiF_0D53REbkZn_sFk
> .
@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:NP155886.RASbdFa8GZHQtkdD6DKTFYLX8_WMiF_0D53REbkZn_sFk130_head
{
this:
np:hasAssertion
dgn-np:NP155886.RASbdFa8GZHQtkdD6DKTFYLX8_WMiF_0D53REbkZn_sFk130_assertion
;
np:hasProvenance
dgn-np:NP155886.RASbdFa8GZHQtkdD6DKTFYLX8_WMiF_0D53REbkZn_sFk130_provenance
;
np:hasPublicationInfo
dgn-np:NP155886.RASbdFa8GZHQtkdD6DKTFYLX8_WMiF_0D53REbkZn_sFk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP155886.RASbdFa8GZHQtkdD6DKTFYLX8_WMiF_0D53REbkZn_sFk130_assertion
a
np:Assertion
.
dgn-np:NP155886.RASbdFa8GZHQtkdD6DKTFYLX8_WMiF_0D53REbkZn_sFk130_provenance
a
np:Provenance
.
dgn-np:NP155886.RASbdFa8GZHQtkdD6DKTFYLX8_WMiF_0D53REbkZn_sFk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP155886.RASbdFa8GZHQtkdD6DKTFYLX8_WMiF_0D53REbkZn_sFk130_assertion
{
miriam-gene:4214
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGNfacd669eec63f54cab2f69d3f17f1468
sio:SIO_000628
miriam-gene:4214
,
lld:C0006142
;
a
sio:SIO_001121
.
}
dgn-np:NP155886.RASbdFa8GZHQtkdD6DKTFYLX8_WMiF_0D53REbkZn_sFk130_provenance
{
dgn-np:NP155886.RASbdFa8GZHQtkdD6DKTFYLX8_WMiF_0D53REbkZn_sFk130_assertion
dcterms:description
"[Recent work from large consortial studies has led to the discovery of novel breast cancer susceptibility loci in genic (CASP8, FGFR2, TNRC9, MAP3K1, LSP1) and nongenic regions (8q24, 2q35, 5p12) of the genome, and to the finding of substantial heterogeneity by tumor characteristics.]. 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:19088016
;
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:NP155886.RASbdFa8GZHQtkdD6DKTFYLX8_WMiF_0D53REbkZn_sFk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:24+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" .
}