@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP299245.RAGb3B28ncyrNBNQGL0VuvTK_4Myy19tMHK-pk4IQwsx0
> .
@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:NP299245.RAGb3B28ncyrNBNQGL0VuvTK_4Myy19tMHK-pk4IQwsx0130_head
{
this:
np:hasAssertion
dgn-np:NP299245.RAGb3B28ncyrNBNQGL0VuvTK_4Myy19tMHK-pk4IQwsx0130_assertion
;
np:hasProvenance
dgn-np:NP299245.RAGb3B28ncyrNBNQGL0VuvTK_4Myy19tMHK-pk4IQwsx0130_provenance
;
np:hasPublicationInfo
dgn-np:NP299245.RAGb3B28ncyrNBNQGL0VuvTK_4Myy19tMHK-pk4IQwsx0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP299245.RAGb3B28ncyrNBNQGL0VuvTK_4Myy19tMHK-pk4IQwsx0130_assertion
a
np:Assertion
.
dgn-np:NP299245.RAGb3B28ncyrNBNQGL0VuvTK_4Myy19tMHK-pk4IQwsx0130_provenance
a
np:Provenance
.
dgn-np:NP299245.RAGb3B28ncyrNBNQGL0VuvTK_4Myy19tMHK-pk4IQwsx0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP299245.RAGb3B28ncyrNBNQGL0VuvTK_4Myy19tMHK-pk4IQwsx0130_assertion
{
miriam-gene:1499
a
ncit:C16612
.
lld:C0025149
a
ncit:C7057
.
dgn-gda:DGN3232ddf6ad70e20bc53696cf1ed64feb
sio:SIO_000628
miriam-gene:1499
,
lld:C0025149
;
a
sio:SIO_001121
.
}
dgn-np:NP299245.RAGb3B28ncyrNBNQGL0VuvTK_4Myy19tMHK-pk4IQwsx0130_provenance
{
dgn-np:NP299245.RAGb3B28ncyrNBNQGL0VuvTK_4Myy19tMHK-pk4IQwsx0130_assertion
dcterms:description
"[APC is a critical component of the Wnt/Wingless signaling pathway, which is disrupted in sporadic cancers (e.g., colorectal adenomas, hepatocellular carcinomas, and medulloblastomas) by somatic mutations affecting multiple genes encoding alternative pathway components, including APC and CTNNB1 (encoding beta-catenin).]. 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:16843107
;
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:NP299245.RAGb3B28ncyrNBNQGL0VuvTK_4Myy19tMHK-pk4IQwsx0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:50+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" .
}