@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP400214.RAOKW4Xpu66LY_zh73VvZl-FMLQfFpoVfiCNdethwP7Tk
> .
@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:NP400214.RAOKW4Xpu66LY_zh73VvZl-FMLQfFpoVfiCNdethwP7Tk130_head
{
this:
np:hasAssertion
dgn-np:NP400214.RAOKW4Xpu66LY_zh73VvZl-FMLQfFpoVfiCNdethwP7Tk130_assertion
;
np:hasProvenance
dgn-np:NP400214.RAOKW4Xpu66LY_zh73VvZl-FMLQfFpoVfiCNdethwP7Tk130_provenance
;
np:hasPublicationInfo
dgn-np:NP400214.RAOKW4Xpu66LY_zh73VvZl-FMLQfFpoVfiCNdethwP7Tk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP400214.RAOKW4Xpu66LY_zh73VvZl-FMLQfFpoVfiCNdethwP7Tk130_assertion
a
np:Assertion
.
dgn-np:NP400214.RAOKW4Xpu66LY_zh73VvZl-FMLQfFpoVfiCNdethwP7Tk130_provenance
a
np:Provenance
.
dgn-np:NP400214.RAOKW4Xpu66LY_zh73VvZl-FMLQfFpoVfiCNdethwP7Tk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP400214.RAOKW4Xpu66LY_zh73VvZl-FMLQfFpoVfiCNdethwP7Tk130_assertion
{
miriam-gene:4360
a
ncit:C16612
.
lld:C0796074
a
ncit:C7057
.
dgn-gda:DGNd527a467ebc978e44f628e9e0c0eeed8
sio:SIO_000628
miriam-gene:4360
,
lld:C0796074
;
a
sio:SIO_001121
.
}
dgn-np:NP400214.RAOKW4Xpu66LY_zh73VvZl-FMLQfFpoVfiCNdethwP7Tk130_provenance
{
dgn-np:NP400214.RAOKW4Xpu66LY_zh73VvZl-FMLQfFpoVfiCNdethwP7Tk130_assertion
dcterms:description
"[Our data suggest that either somatic inactivation of the FHIT gene associated with MSS or inactivation of the MMR system resulting in MSI contribute to the development of periocular SGCs in presumptive MTS.]. 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:16395674
;
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:NP400214.RAOKW4Xpu66LY_zh73VvZl-FMLQfFpoVfiCNdethwP7Tk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:58+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" .
}