@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP397969.RAbhFBbLkuYmQIg0u2x2fGcm_5bWF_OiUPskpk56TcfNk
> .
@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:NP397969.RAbhFBbLkuYmQIg0u2x2fGcm_5bWF_OiUPskpk56TcfNk130_head
{
this:
np:hasAssertion
dgn-np:NP397969.RAbhFBbLkuYmQIg0u2x2fGcm_5bWF_OiUPskpk56TcfNk130_assertion
;
np:hasProvenance
dgn-np:NP397969.RAbhFBbLkuYmQIg0u2x2fGcm_5bWF_OiUPskpk56TcfNk130_provenance
;
np:hasPublicationInfo
dgn-np:NP397969.RAbhFBbLkuYmQIg0u2x2fGcm_5bWF_OiUPskpk56TcfNk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP397969.RAbhFBbLkuYmQIg0u2x2fGcm_5bWF_OiUPskpk56TcfNk130_assertion
a
np:Assertion
.
dgn-np:NP397969.RAbhFBbLkuYmQIg0u2x2fGcm_5bWF_OiUPskpk56TcfNk130_provenance
a
np:Provenance
.
dgn-np:NP397969.RAbhFBbLkuYmQIg0u2x2fGcm_5bWF_OiUPskpk56TcfNk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP397969.RAbhFBbLkuYmQIg0u2x2fGcm_5bWF_OiUPskpk56TcfNk130_assertion
{
miriam-gene:4436
a
ncit:C16612
.
lld:C0014170
a
ncit:C7057
.
dgn-gda:DGN3be75caca779d9fdb5032ba552563340
sio:SIO_000628
miriam-gene:4436
,
lld:C0014170
;
a
sio:SIO_001121
.
}
dgn-np:NP397969.RAbhFBbLkuYmQIg0u2x2fGcm_5bWF_OiUPskpk56TcfNk130_provenance
{
dgn-np:NP397969.RAbhFBbLkuYmQIg0u2x2fGcm_5bWF_OiUPskpk56TcfNk130_assertion
dcterms:description
"[Although a direct relationship between the endometrial cancer susceptibility and the MSH2 mutation we found cannot be established, our observations, consistent with the work of other authors, suggest the involvement of germ line MSH2 abnormalities in endometrial tumor development and support the case for endometrial cancer screening in women from HNPCC families.]. 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:16803540
;
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:NP397969.RAbhFBbLkuYmQIg0u2x2fGcm_5bWF_OiUPskpk56TcfNk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:57+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" .
}