@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP777863.RASuafHAjchqX1km9SA2VfGjRjwtya7ugfDv_BgcXvLNE
> .
@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:NP777863.RASuafHAjchqX1km9SA2VfGjRjwtya7ugfDv_BgcXvLNE130_head
{
this:
np:hasAssertion
dgn-np:NP777863.RASuafHAjchqX1km9SA2VfGjRjwtya7ugfDv_BgcXvLNE130_assertion
;
np:hasProvenance
dgn-np:NP777863.RASuafHAjchqX1km9SA2VfGjRjwtya7ugfDv_BgcXvLNE130_provenance
;
np:hasPublicationInfo
dgn-np:NP777863.RASuafHAjchqX1km9SA2VfGjRjwtya7ugfDv_BgcXvLNE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP777863.RASuafHAjchqX1km9SA2VfGjRjwtya7ugfDv_BgcXvLNE130_assertion
a
np:Assertion
.
dgn-np:NP777863.RASuafHAjchqX1km9SA2VfGjRjwtya7ugfDv_BgcXvLNE130_provenance
a
np:Provenance
.
dgn-np:NP777863.RASuafHAjchqX1km9SA2VfGjRjwtya7ugfDv_BgcXvLNE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP777863.RASuafHAjchqX1km9SA2VfGjRjwtya7ugfDv_BgcXvLNE130_assertion
{
miriam-gene:4360
a
ncit:C16612
.
lld:C0699791
a
ncit:C7057
.
dgn-gda:DGNb56c79ad423a96711ccce3ab7cecb13b
sio:SIO_000628
miriam-gene:4360
,
lld:C0699791
;
a
sio:SIO_001121
.
}
dgn-np:NP777863.RASuafHAjchqX1km9SA2VfGjRjwtya7ugfDv_BgcXvLNE130_provenance
{
dgn-np:NP777863.RASuafHAjchqX1km9SA2VfGjRjwtya7ugfDv_BgcXvLNE130_assertion
dcterms:description
"[Gastric cancer has been observed to be part of the spectrum of neoplasms associated with germline mismatch repair gene (MMR) alterations that give rise to the hereditary nonpolyposis colorectal cancer (HNPCC) entity.]. 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:11979414
;
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:NP777863.RASuafHAjchqX1km9SA2VfGjRjwtya7ugfDv_BgcXvLNE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:51+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" .
}