@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP268468.RAK_7Pk4stlrpYm4yK6AjPVBnQKpoqtcfN3YWTcX0NH-8
> .
@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:NP268468.RAK_7Pk4stlrpYm4yK6AjPVBnQKpoqtcfN3YWTcX0NH-8130_head
{
this:
np:hasAssertion
dgn-np:NP268468.RAK_7Pk4stlrpYm4yK6AjPVBnQKpoqtcfN3YWTcX0NH-8130_assertion
;
np:hasProvenance
dgn-np:NP268468.RAK_7Pk4stlrpYm4yK6AjPVBnQKpoqtcfN3YWTcX0NH-8130_provenance
;
np:hasPublicationInfo
dgn-np:NP268468.RAK_7Pk4stlrpYm4yK6AjPVBnQKpoqtcfN3YWTcX0NH-8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP268468.RAK_7Pk4stlrpYm4yK6AjPVBnQKpoqtcfN3YWTcX0NH-8130_assertion
a
np:Assertion
.
dgn-np:NP268468.RAK_7Pk4stlrpYm4yK6AjPVBnQKpoqtcfN3YWTcX0NH-8130_provenance
a
np:Provenance
.
dgn-np:NP268468.RAK_7Pk4stlrpYm4yK6AjPVBnQKpoqtcfN3YWTcX0NH-8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP268468.RAK_7Pk4stlrpYm4yK6AjPVBnQKpoqtcfN3YWTcX0NH-8130_assertion
{
miriam-gene:6670
a
ncit:C16612
.
lld:C0027831
a
ncit:C7057
.
dgn-gda:DGN7c27adc04f4bac7db0b523b8ef1ab495
sio:SIO_000628
miriam-gene:6670
,
lld:C0027831
;
a
sio:SIO_001121
.
}
dgn-np:NP268468.RAK_7Pk4stlrpYm4yK6AjPVBnQKpoqtcfN3YWTcX0NH-8130_provenance
{
dgn-np:NP268468.RAK_7Pk4stlrpYm4yK6AjPVBnQKpoqtcfN3YWTcX0NH-8130_assertion
dcterms:description
"[The flanking breakpoints of SP3 and API are therefore useful for rapidly localizing new markers to the neurofibromatosis critical region, while the breakpoints of the two translocation patients provide unique opportunities for reverse genetic strategies to clone the NF1 gene.]. 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:2491776
;
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:NP268468.RAK_7Pk4stlrpYm4yK6AjPVBnQKpoqtcfN3YWTcX0NH-8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:30+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" .
}