@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP700694.RApFA_AKPbfxI3B7WTCqL_9xbOpxWBV4_mcFwyUSbmDmI
> .
@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:NP700694.RApFA_AKPbfxI3B7WTCqL_9xbOpxWBV4_mcFwyUSbmDmI130_head
{
this:
np:hasAssertion
dgn-np:NP700694.RApFA_AKPbfxI3B7WTCqL_9xbOpxWBV4_mcFwyUSbmDmI130_assertion
;
np:hasProvenance
dgn-np:NP700694.RApFA_AKPbfxI3B7WTCqL_9xbOpxWBV4_mcFwyUSbmDmI130_provenance
;
np:hasPublicationInfo
dgn-np:NP700694.RApFA_AKPbfxI3B7WTCqL_9xbOpxWBV4_mcFwyUSbmDmI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP700694.RApFA_AKPbfxI3B7WTCqL_9xbOpxWBV4_mcFwyUSbmDmI130_assertion
a
np:Assertion
.
dgn-np:NP700694.RApFA_AKPbfxI3B7WTCqL_9xbOpxWBV4_mcFwyUSbmDmI130_provenance
a
np:Provenance
.
dgn-np:NP700694.RApFA_AKPbfxI3B7WTCqL_9xbOpxWBV4_mcFwyUSbmDmI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP700694.RApFA_AKPbfxI3B7WTCqL_9xbOpxWBV4_mcFwyUSbmDmI130_assertion
{
miriam-gene:4437
a
ncit:C16612
.
lld:C0476089
a
ncit:C7057
.
dgn-gda:DGNf9e956a718cc648e78bd5a3970c5e62f
sio:SIO_000628
miriam-gene:4437
,
lld:C0476089
;
a
sio:SIO_001121
.
}
dgn-np:NP700694.RApFA_AKPbfxI3B7WTCqL_9xbOpxWBV4_mcFwyUSbmDmI130_provenance
{
dgn-np:NP700694.RApFA_AKPbfxI3B7WTCqL_9xbOpxWBV4_mcFwyUSbmDmI130_assertion
dcterms:description
"[We studied the replication error (RER) phenotype in noncoding (Bat-26, Bat-25, D2S123, D5S346, and D17S250) and coding (MSH3, MSH6, BAX, and TGFBR2 genes) DNA sequences, and characterized the germline and somatic mutations of the MSH2 gene in the tumors described above and in endometrial carcinomas from two of her affected siblings.]. 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:15350299
;
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:NP700694.RApFA_AKPbfxI3B7WTCqL_9xbOpxWBV4_mcFwyUSbmDmI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:06+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" .
}