@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP59943.RA4M-XEt6ni9RWGOYqBbWjeIpm7p_SSGAzMSXO-ENF2CI
> .
@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 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:NP59943.RA4M-XEt6ni9RWGOYqBbWjeIpm7p_SSGAzMSXO-ENF2CI130_head
{
this:
np:hasAssertion
dgn-np:NP59943.RA4M-XEt6ni9RWGOYqBbWjeIpm7p_SSGAzMSXO-ENF2CI130_assertion
;
np:hasProvenance
dgn-np:NP59943.RA4M-XEt6ni9RWGOYqBbWjeIpm7p_SSGAzMSXO-ENF2CI130_provenance
;
np:hasPublicationInfo
dgn-np:NP59943.RA4M-XEt6ni9RWGOYqBbWjeIpm7p_SSGAzMSXO-ENF2CI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP59943.RA4M-XEt6ni9RWGOYqBbWjeIpm7p_SSGAzMSXO-ENF2CI130_assertion
a
np:Assertion
.
dgn-np:NP59943.RA4M-XEt6ni9RWGOYqBbWjeIpm7p_SSGAzMSXO-ENF2CI130_provenance
a
np:Provenance
.
dgn-np:NP59943.RA4M-XEt6ni9RWGOYqBbWjeIpm7p_SSGAzMSXO-ENF2CI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP59943.RA4M-XEt6ni9RWGOYqBbWjeIpm7p_SSGAzMSXO-ENF2CI130_assertion
{
miriam-gene:1312
a
ncit:C16612
.
lld:C1846502
a
ncit:C7057
.
dgn-gda:DGN1030231fe705cdca7a0c449b023a4523
sio:SIO_000628
miriam-gene:1312
,
lld:C1846502
;
a
sio:SIO_001122
.
}
dgn-np:NP59943.RA4M-XEt6ni9RWGOYqBbWjeIpm7p_SSGAzMSXO-ENF2CI130_provenance
{
dgn-np:NP59943.RA4M-XEt6ni9RWGOYqBbWjeIpm7p_SSGAzMSXO-ENF2CI130_assertion
dct:description
"[Our data suggest lower mammographic density for women carrying the COMT and CYP1A2 variant alleles than for women carrying the common alleles, though this is the opposite of what is commonly hypothesized from the enzyme function.]. 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:15382051
;
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:NP59943.RA4M-XEt6ni9RWGOYqBbWjeIpm7p_SSGAzMSXO-ENF2CI130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:28+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}