@prefix semsc: <
http://semanticscience.org/resource/
> .
@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP209075.RACJIYDL6PpYqJdVjKH1naRcVR3Uo_r22KNDxxHsnqNwo
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@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 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:NP209075.RACJIYDL6PpYqJdVjKH1naRcVR3Uo_r22KNDxxHsnqNwo130_head
{
this:
np:hasAssertion
dgn-np:NP209075.RACJIYDL6PpYqJdVjKH1naRcVR3Uo_r22KNDxxHsnqNwo130_assertion
;
np:hasProvenance
dgn-np:NP209075.RACJIYDL6PpYqJdVjKH1naRcVR3Uo_r22KNDxxHsnqNwo130_provenance
;
np:hasPublicationInfo
dgn-np:NP209075.RACJIYDL6PpYqJdVjKH1naRcVR3Uo_r22KNDxxHsnqNwo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP209075.RACJIYDL6PpYqJdVjKH1naRcVR3Uo_r22KNDxxHsnqNwo130_assertion
a
np:Assertion
.
dgn-np:NP209075.RACJIYDL6PpYqJdVjKH1naRcVR3Uo_r22KNDxxHsnqNwo130_provenance
a
np:Provenance
.
dgn-np:NP209075.RACJIYDL6PpYqJdVjKH1naRcVR3Uo_r22KNDxxHsnqNwo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP209075.RACJIYDL6PpYqJdVjKH1naRcVR3Uo_r22KNDxxHsnqNwo130_assertion
{
miriam-gene:4000
a
ncit:C16612
.
lld:C0033300
a
ncit:C7057
.
dgn-gda:DGNab793f720d6e4f136d51855eb2852895
semsc:SIO_000628
miriam-gene:4000
,
lld:C0033300
;
a
semsc:SIO_001121
.
}
dgn-np:NP209075.RACJIYDL6PpYqJdVjKH1naRcVR3Uo_r22KNDxxHsnqNwo130_provenance
{
dgn-np:NP209075.RACJIYDL6PpYqJdVjKH1naRcVR3Uo_r22KNDxxHsnqNwo130_assertion
dct:description
"[One of the major breakthroughs both in the lamin field and for this syndrome is that many of the cellular defects observed in HGPS patient cells and model systems can be restored after treatment with a class of compounds known as FTIs (farnesyltransferase inhibitors).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
semsc:SIO_000772
miriam-pubmed:20074076
;
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:NP209075.RACJIYDL6PpYqJdVjKH1naRcVR3Uo_r22KNDxxHsnqNwo130_publicationInfo
{
this:
dct:created
"2014-10-02T12:33:55+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
semsc:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}