@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP371668.RAQJfCsLeOh2tKjGF55pnmABTwK1xu2Nklad4FzcWxmUA
> .
@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:NP371668.RAQJfCsLeOh2tKjGF55pnmABTwK1xu2Nklad4FzcWxmUA130_head
{
this:
np:hasAssertion
dgn-np:NP371668.RAQJfCsLeOh2tKjGF55pnmABTwK1xu2Nklad4FzcWxmUA130_assertion
;
np:hasProvenance
dgn-np:NP371668.RAQJfCsLeOh2tKjGF55pnmABTwK1xu2Nklad4FzcWxmUA130_provenance
;
np:hasPublicationInfo
dgn-np:NP371668.RAQJfCsLeOh2tKjGF55pnmABTwK1xu2Nklad4FzcWxmUA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP371668.RAQJfCsLeOh2tKjGF55pnmABTwK1xu2Nklad4FzcWxmUA130_assertion
a
np:Assertion
.
dgn-np:NP371668.RAQJfCsLeOh2tKjGF55pnmABTwK1xu2Nklad4FzcWxmUA130_provenance
a
np:Provenance
.
dgn-np:NP371668.RAQJfCsLeOh2tKjGF55pnmABTwK1xu2Nklad4FzcWxmUA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP371668.RAQJfCsLeOh2tKjGF55pnmABTwK1xu2Nklad4FzcWxmUA130_assertion
{
miriam-gene:4436
a
ncit:C16612
.
lld:C0334381
a
ncit:C7057
.
dgn-gda:DGN68a4c6f1cb15c7ffd02ff7e8d6fef04a
sio:SIO_000628
miriam-gene:4436
,
lld:C0334381
;
a
sio:SIO_001121
.
}
dgn-np:NP371668.RAQJfCsLeOh2tKjGF55pnmABTwK1xu2Nklad4FzcWxmUA130_provenance
{
dgn-np:NP371668.RAQJfCsLeOh2tKjGF55pnmABTwK1xu2Nklad4FzcWxmUA130_assertion
dcterms:description
"[The high frequency of microsatellite instability in lobular breast cancers, coupled with increased risk of breast cancer associated with germline mismatch repair gene mutations raises the possibility that mutations MSH2 or MLH1 might confer susceptibility to LCIS.]. 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:11369138
;
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:NP371668.RAQJfCsLeOh2tKjGF55pnmABTwK1xu2Nklad4FzcWxmUA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:37+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" .
}