@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP53952.RAyxpLBetUrUCiPO34K6rjaT0QJNuRpz9o69BcRGrbB1A
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP53952.RAyxpLBetUrUCiPO34K6rjaT0QJNuRpz9o69BcRGrbB1A130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP53952.RAyxpLBetUrUCiPO34K6rjaT0QJNuRpz9o69BcRGrbB1A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP53952.RAyxpLBetUrUCiPO34K6rjaT0QJNuRpz9o69BcRGrbB1A130_assertion
a
np:Assertion
.
dgn-np:NP53952.RAyxpLBetUrUCiPO34K6rjaT0QJNuRpz9o69BcRGrbB1A130_provenance
a
np:Provenance
.
dgn-np:NP53952.RAyxpLBetUrUCiPO34K6rjaT0QJNuRpz9o69BcRGrbB1A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP53952.RAyxpLBetUrUCiPO34K6rjaT0QJNuRpz9o69BcRGrbB1A130_assertion
{
miriam-gene:8202
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGN7a159647abd67d098ea43fbf1a5d5731
sio:SIO_000628
miriam-gene:8202
,
lld:C0006142
;
a
sio:SIO_001122
.
}
dgn-np:NP53952.RAyxpLBetUrUCiPO34K6rjaT0QJNuRpz9o69BcRGrbB1A130_provenance
{
dgn-np:NP53952.RAyxpLBetUrUCiPO34K6rjaT0QJNuRpz9o69BcRGrbB1A130_assertion
dcterms:description
"[These results strongly suggest that contrary to previous studies, there is no significant effect of AIB1 genetic variation on BC risk in BRCA1 mutation carriers and provide an indication that there is also no strong risk modification in BRCA2 carriers.]. 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:15900600
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP53952.RAyxpLBetUrUCiPO34K6rjaT0QJNuRpz9o69BcRGrbB1A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:25+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" .
}