@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP885191.RAQlIEqvtRuaqcQfpzeJnsxWCohh9t1T8G4MlH8QFsSFs
> .
@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:NP885191.RAQlIEqvtRuaqcQfpzeJnsxWCohh9t1T8G4MlH8QFsSFs130_head
{
this:
np:hasAssertion
dgn-np:NP885191.RAQlIEqvtRuaqcQfpzeJnsxWCohh9t1T8G4MlH8QFsSFs130_assertion
;
np:hasProvenance
dgn-np:NP885191.RAQlIEqvtRuaqcQfpzeJnsxWCohh9t1T8G4MlH8QFsSFs130_provenance
;
np:hasPublicationInfo
dgn-np:NP885191.RAQlIEqvtRuaqcQfpzeJnsxWCohh9t1T8G4MlH8QFsSFs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP885191.RAQlIEqvtRuaqcQfpzeJnsxWCohh9t1T8G4MlH8QFsSFs130_assertion
a
np:Assertion
.
dgn-np:NP885191.RAQlIEqvtRuaqcQfpzeJnsxWCohh9t1T8G4MlH8QFsSFs130_provenance
a
np:Provenance
.
dgn-np:NP885191.RAQlIEqvtRuaqcQfpzeJnsxWCohh9t1T8G4MlH8QFsSFs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP885191.RAQlIEqvtRuaqcQfpzeJnsxWCohh9t1T8G4MlH8QFsSFs130_assertion
{
miriam-gene:4803
a
ncit:C16612
.
lld:C0025149
a
ncit:C7057
.
dgn-gda:DGNffeb5faca25d199b4fa579ed55957469
sio:SIO_000628
miriam-gene:4803
,
lld:C0025149
;
a
sio:SIO_001121
.
}
dgn-np:NP885191.RAQlIEqvtRuaqcQfpzeJnsxWCohh9t1T8G4MlH8QFsSFs130_provenance
{
dgn-np:NP885191.RAQlIEqvtRuaqcQfpzeJnsxWCohh9t1T8G4MlH8QFsSFs130_assertion
dcterms:description
"[Since the inability to respond appropriately to differentiation factors such as NGF may contribute to determining the malignant phenotype of neuroblastomas, we sought to determine whether the same is true of medulloblastomas.]. 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:2172988
;
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:NP885191.RAQlIEqvtRuaqcQfpzeJnsxWCohh9t1T8G4MlH8QFsSFs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:00+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" .
}