@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP196972.RAAI9_ZYhOpej5qFTpLd5gdPXpIG56LuWAlfBR1IclZOA
> .
@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:NP196972.RAAI9_ZYhOpej5qFTpLd5gdPXpIG56LuWAlfBR1IclZOA130_head
{
this:
np:hasAssertion
dgn-np:NP196972.RAAI9_ZYhOpej5qFTpLd5gdPXpIG56LuWAlfBR1IclZOA130_assertion
;
np:hasProvenance
dgn-np:NP196972.RAAI9_ZYhOpej5qFTpLd5gdPXpIG56LuWAlfBR1IclZOA130_provenance
;
np:hasPublicationInfo
dgn-np:NP196972.RAAI9_ZYhOpej5qFTpLd5gdPXpIG56LuWAlfBR1IclZOA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP196972.RAAI9_ZYhOpej5qFTpLd5gdPXpIG56LuWAlfBR1IclZOA130_assertion
a
np:Assertion
.
dgn-np:NP196972.RAAI9_ZYhOpej5qFTpLd5gdPXpIG56LuWAlfBR1IclZOA130_provenance
a
np:Provenance
.
dgn-np:NP196972.RAAI9_ZYhOpej5qFTpLd5gdPXpIG56LuWAlfBR1IclZOA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP196972.RAAI9_ZYhOpej5qFTpLd5gdPXpIG56LuWAlfBR1IclZOA130_assertion
{
miriam-gene:1312
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGN0e7a037adab982b457e8726980a2dbeb
sio:SIO_000628
miriam-gene:1312
,
lld:C0006142
;
a
sio:SIO_001121
.
}
dgn-np:NP196972.RAAI9_ZYhOpej5qFTpLd5gdPXpIG56LuWAlfBR1IclZOA130_provenance
{
dgn-np:NP196972.RAAI9_ZYhOpej5qFTpLd5gdPXpIG56LuWAlfBR1IclZOA130_assertion
dcterms:description
"[Although the study found that parental carrier status of certain CYP1B1 or COMT genotypes might be associated with daughter's breast cancer risk, the biological basis as well as independent confirmation of this finding need to be investigated in future larger family-based studies before making meaningful inferences.]. 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:15111770
;
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:NP196972.RAAI9_ZYhOpej5qFTpLd5gdPXpIG56LuWAlfBR1IclZOA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:48+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" .
}