@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP561602.RAX8883NgkzWEICQ9BH84hrEyS0M2GM2o0OJmP8lmAknE
> .
@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:NP561602.RAX8883NgkzWEICQ9BH84hrEyS0M2GM2o0OJmP8lmAknE130_head
{
this:
np:hasAssertion
dgn-np:NP561602.RAX8883NgkzWEICQ9BH84hrEyS0M2GM2o0OJmP8lmAknE130_assertion
;
np:hasProvenance
dgn-np:NP561602.RAX8883NgkzWEICQ9BH84hrEyS0M2GM2o0OJmP8lmAknE130_provenance
;
np:hasPublicationInfo
dgn-np:NP561602.RAX8883NgkzWEICQ9BH84hrEyS0M2GM2o0OJmP8lmAknE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP561602.RAX8883NgkzWEICQ9BH84hrEyS0M2GM2o0OJmP8lmAknE130_assertion
a
np:Assertion
.
dgn-np:NP561602.RAX8883NgkzWEICQ9BH84hrEyS0M2GM2o0OJmP8lmAknE130_provenance
a
np:Provenance
.
dgn-np:NP561602.RAX8883NgkzWEICQ9BH84hrEyS0M2GM2o0OJmP8lmAknE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP561602.RAX8883NgkzWEICQ9BH84hrEyS0M2GM2o0OJmP8lmAknE130_assertion
{
miriam-gene:4763
a
ncit:C16612
.
lld:C0019562
a
ncit:C7057
.
dgn-gda:DGN8704a5eeb4b971688c054d88af0e7004
sio:SIO_000628
miriam-gene:4763
,
lld:C0019562
;
a
sio:SIO_001121
.
}
dgn-np:NP561602.RAX8883NgkzWEICQ9BH84hrEyS0M2GM2o0OJmP8lmAknE130_provenance
{
dgn-np:NP561602.RAX8883NgkzWEICQ9BH84hrEyS0M2GM2o0OJmP8lmAknE130_assertion
dcterms:description
"[We now know that TSC is a hamartomatosis, and thanks to studies of recent years using positional cloning and DNA analysis, we are beginning to understand the biological mechanisms of these disorders which include NF1, NF2 and von Hippel-Lindau disease.]. 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:8882573
;
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:NP561602.RAX8883NgkzWEICQ9BH84hrEyS0M2GM2o0OJmP8lmAknE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:38+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" .
}