@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP683884.RAzTX2Ua44696zWVrQ-GQRt9YjrEdgjEp9LX-Ot-DHoSs
> .
@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:NP683884.RAzTX2Ua44696zWVrQ-GQRt9YjrEdgjEp9LX-Ot-DHoSs130_head
{
this:
np:hasAssertion
dgn-np:NP683884.RAzTX2Ua44696zWVrQ-GQRt9YjrEdgjEp9LX-Ot-DHoSs130_assertion
;
np:hasProvenance
dgn-np:NP683884.RAzTX2Ua44696zWVrQ-GQRt9YjrEdgjEp9LX-Ot-DHoSs130_provenance
;
np:hasPublicationInfo
dgn-np:NP683884.RAzTX2Ua44696zWVrQ-GQRt9YjrEdgjEp9LX-Ot-DHoSs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP683884.RAzTX2Ua44696zWVrQ-GQRt9YjrEdgjEp9LX-Ot-DHoSs130_assertion
a
np:Assertion
.
dgn-np:NP683884.RAzTX2Ua44696zWVrQ-GQRt9YjrEdgjEp9LX-Ot-DHoSs130_provenance
a
np:Provenance
.
dgn-np:NP683884.RAzTX2Ua44696zWVrQ-GQRt9YjrEdgjEp9LX-Ot-DHoSs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP683884.RAzTX2Ua44696zWVrQ-GQRt9YjrEdgjEp9LX-Ot-DHoSs130_assertion
{
miriam-gene:30061
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGN2614ee1b0093b14f88bc30da736cf15a
sio:SIO_000628
miriam-gene:30061
,
lld:C0006142
;
a
sio:SIO_001121
.
}
dgn-np:NP683884.RAzTX2Ua44696zWVrQ-GQRt9YjrEdgjEp9LX-Ot-DHoSs130_provenance
{
dgn-np:NP683884.RAzTX2Ua44696zWVrQ-GQRt9YjrEdgjEp9LX-Ot-DHoSs130_assertion
dcterms:description
"[To understand the role of hemochromatosis and transferrin receptor system mutations in breast cancer, we analyzed 19 sequence variations at HFE, TFR1, TFR2, and FPN1 and compared genotype frequencies between cases and controls in a German population.]. 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:15894659
;
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:NP683884.RAzTX2Ua44696zWVrQ-GQRt9YjrEdgjEp9LX-Ot-DHoSs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:55+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" .
}