@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP925981.RAadlNUZAB5OZ9EIXNpG9_5bZ_XAl7Ybnoi0ucrBq4hbQ
> .
@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:NP925981.RAadlNUZAB5OZ9EIXNpG9_5bZ_XAl7Ybnoi0ucrBq4hbQ130_head
{
this:
np:hasAssertion
dgn-np:NP925981.RAadlNUZAB5OZ9EIXNpG9_5bZ_XAl7Ybnoi0ucrBq4hbQ130_assertion
;
np:hasProvenance
dgn-np:NP925981.RAadlNUZAB5OZ9EIXNpG9_5bZ_XAl7Ybnoi0ucrBq4hbQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP925981.RAadlNUZAB5OZ9EIXNpG9_5bZ_XAl7Ybnoi0ucrBq4hbQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP925981.RAadlNUZAB5OZ9EIXNpG9_5bZ_XAl7Ybnoi0ucrBq4hbQ130_assertion
a
np:Assertion
.
dgn-np:NP925981.RAadlNUZAB5OZ9EIXNpG9_5bZ_XAl7Ybnoi0ucrBq4hbQ130_provenance
a
np:Provenance
.
dgn-np:NP925981.RAadlNUZAB5OZ9EIXNpG9_5bZ_XAl7Ybnoi0ucrBq4hbQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP925981.RAadlNUZAB5OZ9EIXNpG9_5bZ_XAl7Ybnoi0ucrBq4hbQ130_assertion
{
miriam-gene:5979
a
ncit:C16612
.
lld:C0017075
a
ncit:C7057
.
dgn-gda:DGNa8ab369c8441bfd990a2de59f0059306
sio:SIO_000628
miriam-gene:5979
,
lld:C0017075
;
a
sio:SIO_001121
.
}
dgn-np:NP925981.RAadlNUZAB5OZ9EIXNpG9_5bZ_XAl7Ybnoi0ucrBq4hbQ130_provenance
{
dgn-np:NP925981.RAadlNUZAB5OZ9EIXNpG9_5bZ_XAl7Ybnoi0ucrBq4hbQ130_assertion
dcterms:description
"[In addition to associations with neuroblastoma and tumours related to MEN2B, HSCR may also be associated with tumours of neural origin such as ganglioneuroma, ganglioneuroblastoma, retinoblastoma and tumours associated with neurofibromatosis and other autonomic nervous system disturbances.]. 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:16518596
;
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:NP925981.RAadlNUZAB5OZ9EIXNpG9_5bZ_XAl7Ybnoi0ucrBq4hbQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:28+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" .
}