@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP709926.RA995sjT75_2x2yqbbv77IhE8JwsR6qAm1L56iPKaymH0
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP709926.RA995sjT75_2x2yqbbv77IhE8JwsR6qAm1L56iPKaymH0130_head
{
this:
np:hasAssertion
dgn-np:NP709926.RA995sjT75_2x2yqbbv77IhE8JwsR6qAm1L56iPKaymH0130_assertion
;
np:hasProvenance
dgn-np:NP709926.RA995sjT75_2x2yqbbv77IhE8JwsR6qAm1L56iPKaymH0130_provenance
;
np:hasPublicationInfo
dgn-np:NP709926.RA995sjT75_2x2yqbbv77IhE8JwsR6qAm1L56iPKaymH0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP709926.RA995sjT75_2x2yqbbv77IhE8JwsR6qAm1L56iPKaymH0130_assertion
a
np:Assertion
.
dgn-np:NP709926.RA995sjT75_2x2yqbbv77IhE8JwsR6qAm1L56iPKaymH0130_provenance
a
np:Provenance
.
dgn-np:NP709926.RA995sjT75_2x2yqbbv77IhE8JwsR6qAm1L56iPKaymH0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP709926.RA995sjT75_2x2yqbbv77IhE8JwsR6qAm1L56iPKaymH0130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0678222
a
ncit:C7057
.
dgn-gda:DGN6c6a7ce44d9c07b599332d0ad79a859a
sio:SIO_000628
miriam-gene:7157
,
lld:C0678222
;
a
sio:SIO_001121
.
}
dgn-np:NP709926.RA995sjT75_2x2yqbbv77IhE8JwsR6qAm1L56iPKaymH0130_provenance
{
dgn-np:NP709926.RA995sjT75_2x2yqbbv77IhE8JwsR6qAm1L56iPKaymH0130_assertion
dcterms:description
"[Except for the high breast cancer risk in BRCA1 and BRCA2 mutation carriers as well as the risk for breast cancer in certain rare syndromes caused by mutations in TP53, STK11, PTEN, CDH1, NF1 or NBN, familial clustering of breast cancer remains largely unexplained.]. 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:19092773
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP709926.RA995sjT75_2x2yqbbv77IhE8JwsR6qAm1L56iPKaymH0130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:07+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}