@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP112216.RA46zSq8exPxkvz2aGHApl77wLyQqyrHm8fuoAXMG50Sc
> .
@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:NP112216.RA46zSq8exPxkvz2aGHApl77wLyQqyrHm8fuoAXMG50Sc130_head
{
this:
np:hasAssertion
dgn-np:NP112216.RA46zSq8exPxkvz2aGHApl77wLyQqyrHm8fuoAXMG50Sc130_assertion
;
np:hasProvenance
dgn-np:NP112216.RA46zSq8exPxkvz2aGHApl77wLyQqyrHm8fuoAXMG50Sc130_provenance
;
np:hasPublicationInfo
dgn-np:NP112216.RA46zSq8exPxkvz2aGHApl77wLyQqyrHm8fuoAXMG50Sc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP112216.RA46zSq8exPxkvz2aGHApl77wLyQqyrHm8fuoAXMG50Sc130_assertion
a
np:Assertion
.
dgn-np:NP112216.RA46zSq8exPxkvz2aGHApl77wLyQqyrHm8fuoAXMG50Sc130_provenance
a
np:Provenance
.
dgn-np:NP112216.RA46zSq8exPxkvz2aGHApl77wLyQqyrHm8fuoAXMG50Sc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP112216.RA46zSq8exPxkvz2aGHApl77wLyQqyrHm8fuoAXMG50Sc130_assertion
{
miriam-gene:672
a
ncit:C16612
.
lld:C0027651
a
ncit:C7057
.
dgn-gda:DGN959fc2c97cb285ead90f08b888f9c032
sio:SIO_000628
miriam-gene:672
,
lld:C0027651
;
a
sio:SIO_001122
.
}
dgn-np:NP112216.RA46zSq8exPxkvz2aGHApl77wLyQqyrHm8fuoAXMG50Sc130_provenance
{
dgn-np:NP112216.RA46zSq8exPxkvz2aGHApl77wLyQqyrHm8fuoAXMG50Sc130_assertion
dcterms:description
"[Ninteen percent of the women who developed both invasive breast and ovarian tumors carried one of the analyzed BRCA1 gene mutations but none of the women were positive for the analyzed BRCA2 mutation.]. 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:16944270
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP112216.RA46zSq8exPxkvz2aGHApl77wLyQqyrHm8fuoAXMG50Sc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:57+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" .
}