@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP747954.RACq7MpP7LjIPBgEjVwzY7D2nIn8pMTy2k9ORXfvgtG-Q
> .
@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:NP747954.RACq7MpP7LjIPBgEjVwzY7D2nIn8pMTy2k9ORXfvgtG-Q130_head
{
this:
np:hasAssertion
dgn-np:NP747954.RACq7MpP7LjIPBgEjVwzY7D2nIn8pMTy2k9ORXfvgtG-Q130_assertion
;
np:hasProvenance
dgn-np:NP747954.RACq7MpP7LjIPBgEjVwzY7D2nIn8pMTy2k9ORXfvgtG-Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP747954.RACq7MpP7LjIPBgEjVwzY7D2nIn8pMTy2k9ORXfvgtG-Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP747954.RACq7MpP7LjIPBgEjVwzY7D2nIn8pMTy2k9ORXfvgtG-Q130_assertion
a
np:Assertion
.
dgn-np:NP747954.RACq7MpP7LjIPBgEjVwzY7D2nIn8pMTy2k9ORXfvgtG-Q130_provenance
a
np:Provenance
.
dgn-np:NP747954.RACq7MpP7LjIPBgEjVwzY7D2nIn8pMTy2k9ORXfvgtG-Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP747954.RACq7MpP7LjIPBgEjVwzY7D2nIn8pMTy2k9ORXfvgtG-Q130_assertion
{
miriam-gene:5728
a
ncit:C16612
.
lld:C0007104
a
ncit:C7057
.
dgn-gda:DGN8590eb64b83b1a67d51ce1a8366e603a
sio:SIO_000628
miriam-gene:5728
,
lld:C0007104
;
a
sio:SIO_001121
.
}
dgn-np:NP747954.RACq7MpP7LjIPBgEjVwzY7D2nIn8pMTy2k9ORXfvgtG-Q130_provenance
{
dgn-np:NP747954.RACq7MpP7LjIPBgEjVwzY7D2nIn8pMTy2k9ORXfvgtG-Q130_assertion
dcterms:description
"[These two cases of male breast cancer associated with germline PTEN mutations and the CS phenotype suggest that CS may be associated with an increased risk of early onset male as well as female 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:11238682
;
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:NP747954.RACq7MpP7LjIPBgEjVwzY7D2nIn8pMTy2k9ORXfvgtG-Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:33+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" .
}