@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP905173.RAKwwpaD0xte-D9IHc4kqaRwRo-OiUoBNlrnEloCa46wo
> .
@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:NP905173.RAKwwpaD0xte-D9IHc4kqaRwRo-OiUoBNlrnEloCa46wo130_head
{
this:
np:hasAssertion
dgn-np:NP905173.RAKwwpaD0xte-D9IHc4kqaRwRo-OiUoBNlrnEloCa46wo130_assertion
;
np:hasProvenance
dgn-np:NP905173.RAKwwpaD0xte-D9IHc4kqaRwRo-OiUoBNlrnEloCa46wo130_provenance
;
np:hasPublicationInfo
dgn-np:NP905173.RAKwwpaD0xte-D9IHc4kqaRwRo-OiUoBNlrnEloCa46wo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP905173.RAKwwpaD0xte-D9IHc4kqaRwRo-OiUoBNlrnEloCa46wo130_assertion
a
np:Assertion
.
dgn-np:NP905173.RAKwwpaD0xte-D9IHc4kqaRwRo-OiUoBNlrnEloCa46wo130_provenance
a
np:Provenance
.
dgn-np:NP905173.RAKwwpaD0xte-D9IHc4kqaRwRo-OiUoBNlrnEloCa46wo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP905173.RAKwwpaD0xte-D9IHc4kqaRwRo-OiUoBNlrnEloCa46wo130_assertion
{
miriam-gene:5624
a
ncit:C16612
.
lld:C2939420
a
ncit:C7057
.
dgn-gda:DGN02efc0069f34560d642a6e32f4a9b9b6
sio:SIO_000628
miriam-gene:5624
,
lld:C2939420
;
a
sio:SIO_001121
.
}
dgn-np:NP905173.RAKwwpaD0xte-D9IHc4kqaRwRo-OiUoBNlrnEloCa46wo130_provenance
{
dgn-np:NP905173.RAKwwpaD0xte-D9IHc4kqaRwRo-OiUoBNlrnEloCa46wo130_assertion
dcterms:description
"[Our hypothesis, which has received recent experimental support, is that the mechanism that links abnormalities at the gene level (eg, APC mutations) and abnormalities at the tissue level (eg, proliferative shift, dysplasia, carcinoma) from cancer initiation to metastasis is SC overpopulation.]. 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:18539961
;
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:NP905173.RAKwwpaD0xte-D9IHc4kqaRwRo-OiUoBNlrnEloCa46wo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:16+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" .
}