@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP610233.RALr3kfd2wp4xfbSdgtW1PwOHcfhved2VOB30ZYn9CFHk
> .
@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:NP610233.RALr3kfd2wp4xfbSdgtW1PwOHcfhved2VOB30ZYn9CFHk130_head
{
this:
np:hasAssertion
dgn-np:NP610233.RALr3kfd2wp4xfbSdgtW1PwOHcfhved2VOB30ZYn9CFHk130_assertion
;
np:hasProvenance
dgn-np:NP610233.RALr3kfd2wp4xfbSdgtW1PwOHcfhved2VOB30ZYn9CFHk130_provenance
;
np:hasPublicationInfo
dgn-np:NP610233.RALr3kfd2wp4xfbSdgtW1PwOHcfhved2VOB30ZYn9CFHk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP610233.RALr3kfd2wp4xfbSdgtW1PwOHcfhved2VOB30ZYn9CFHk130_assertion
a
np:Assertion
.
dgn-np:NP610233.RALr3kfd2wp4xfbSdgtW1PwOHcfhved2VOB30ZYn9CFHk130_provenance
a
np:Provenance
.
dgn-np:NP610233.RALr3kfd2wp4xfbSdgtW1PwOHcfhved2VOB30ZYn9CFHk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP610233.RALr3kfd2wp4xfbSdgtW1PwOHcfhved2VOB30ZYn9CFHk130_assertion
{
miriam-gene:8045
a
ncit:C16612
.
lld:C0678222
a
ncit:C7057
.
dgn-gda:DGNb801e3fac822e6e8891038990cd60eb0
sio:SIO_000628
miriam-gene:8045
,
lld:C0678222
;
a
sio:SIO_001121
.
}
dgn-np:NP610233.RALr3kfd2wp4xfbSdgtW1PwOHcfhved2VOB30ZYn9CFHk130_provenance
{
dgn-np:NP610233.RALr3kfd2wp4xfbSdgtW1PwOHcfhved2VOB30ZYn9CFHk130_assertion
dcterms:description
"[A recent meta-analysis of 23 studies supported the empirically derived hypothesis that women who lack one of the four common minisatellite alleles at the HRAS1 locus are at increased risk of breast cancer.]. 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:10601382
;
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:NP610233.RALr3kfd2wp4xfbSdgtW1PwOHcfhved2VOB30ZYn9CFHk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:06+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" .
}