@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP385229.RAtTB4K16PLiZ4UfvZEuJoh2s9g6sOI4LGeFLdhWpn4e4
> .
@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:NP385229.RAtTB4K16PLiZ4UfvZEuJoh2s9g6sOI4LGeFLdhWpn4e4130_head
{
this:
np:hasAssertion
dgn-np:NP385229.RAtTB4K16PLiZ4UfvZEuJoh2s9g6sOI4LGeFLdhWpn4e4130_assertion
;
np:hasProvenance
dgn-np:NP385229.RAtTB4K16PLiZ4UfvZEuJoh2s9g6sOI4LGeFLdhWpn4e4130_provenance
;
np:hasPublicationInfo
dgn-np:NP385229.RAtTB4K16PLiZ4UfvZEuJoh2s9g6sOI4LGeFLdhWpn4e4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP385229.RAtTB4K16PLiZ4UfvZEuJoh2s9g6sOI4LGeFLdhWpn4e4130_assertion
a
np:Assertion
.
dgn-np:NP385229.RAtTB4K16PLiZ4UfvZEuJoh2s9g6sOI4LGeFLdhWpn4e4130_provenance
a
np:Provenance
.
dgn-np:NP385229.RAtTB4K16PLiZ4UfvZEuJoh2s9g6sOI4LGeFLdhWpn4e4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP385229.RAtTB4K16PLiZ4UfvZEuJoh2s9g6sOI4LGeFLdhWpn4e4130_assertion
{
miriam-gene:4193
a
ncit:C16612
.
lld:C0678222
a
ncit:C7057
.
dgn-gda:DGN0966d9877febad17f2c541c5f34dd37f
sio:SIO_000628
miriam-gene:4193
,
lld:C0678222
;
a
sio:SIO_001121
.
}
dgn-np:NP385229.RAtTB4K16PLiZ4UfvZEuJoh2s9g6sOI4LGeFLdhWpn4e4130_provenance
{
dgn-np:NP385229.RAtTB4K16PLiZ4UfvZEuJoh2s9g6sOI4LGeFLdhWpn4e4130_assertion
dcterms:description
"[Together, the data suggest that though the MDM2 SNP309 G allele is a risk factor for breast cancer, it does not accelerate, but delays the onset of the sporadic disease in Chinese women, highlighting that differences in ethnicity and family history may influence the role of MDM2 SNP309 in cancer susceptibility.]. 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:18281248
;
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:NP385229.RAtTB4K16PLiZ4UfvZEuJoh2s9g6sOI4LGeFLdhWpn4e4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:49+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" .
}