@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP708157.RAr-E5VLf2QDN_XMi04cz6aI5hwfcin0kMBI8_IUH3-gg
> .
@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:NP708157.RAr-E5VLf2QDN_XMi04cz6aI5hwfcin0kMBI8_IUH3-gg130_head
{
this:
np:hasAssertion
dgn-np:NP708157.RAr-E5VLf2QDN_XMi04cz6aI5hwfcin0kMBI8_IUH3-gg130_assertion
;
np:hasProvenance
dgn-np:NP708157.RAr-E5VLf2QDN_XMi04cz6aI5hwfcin0kMBI8_IUH3-gg130_provenance
;
np:hasPublicationInfo
dgn-np:NP708157.RAr-E5VLf2QDN_XMi04cz6aI5hwfcin0kMBI8_IUH3-gg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP708157.RAr-E5VLf2QDN_XMi04cz6aI5hwfcin0kMBI8_IUH3-gg130_assertion
a
np:Assertion
.
dgn-np:NP708157.RAr-E5VLf2QDN_XMi04cz6aI5hwfcin0kMBI8_IUH3-gg130_provenance
a
np:Provenance
.
dgn-np:NP708157.RAr-E5VLf2QDN_XMi04cz6aI5hwfcin0kMBI8_IUH3-gg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP708157.RAr-E5VLf2QDN_XMi04cz6aI5hwfcin0kMBI8_IUH3-gg130_assertion
{
miriam-gene:2523
a
ncit:C16612
.
lld:C3463824
a
ncit:C7057
.
dgn-gda:DGNc2aab578d3544ecc2f1bee903ae11349
sio:SIO_000628
miriam-gene:2523
,
lld:C3463824
;
a
sio:SIO_001121
.
}
dgn-np:NP708157.RAr-E5VLf2QDN_XMi04cz6aI5hwfcin0kMBI8_IUH3-gg130_provenance
{
dgn-np:NP708157.RAr-E5VLf2QDN_XMi04cz6aI5hwfcin0kMBI8_IUH3-gg130_assertion
dcterms:description
"[These data provide a cautionary note for HSC-expansion strategies through Wnt pathway activation, provide evidence that cell extrinsic factors can contribute to the development of myeloid disease, and indicate that loss of function of APC may contribute to the phenotype observed in patients with MDS and del(5q).]. 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:20197553
;
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:NP708157.RAr-E5VLf2QDN_XMi04cz6aI5hwfcin0kMBI8_IUH3-gg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:10+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" .
}