@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP722047.RAVXrLuoBNZS65yUc6FDKj-8dRRVHKHKz1udAri-Uewag
> .
@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:NP722047.RAVXrLuoBNZS65yUc6FDKj-8dRRVHKHKz1udAri-Uewag130_head
{
this:
np:hasAssertion
dgn-np:NP722047.RAVXrLuoBNZS65yUc6FDKj-8dRRVHKHKz1udAri-Uewag130_assertion
;
np:hasProvenance
dgn-np:NP722047.RAVXrLuoBNZS65yUc6FDKj-8dRRVHKHKz1udAri-Uewag130_provenance
;
np:hasPublicationInfo
dgn-np:NP722047.RAVXrLuoBNZS65yUc6FDKj-8dRRVHKHKz1udAri-Uewag130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP722047.RAVXrLuoBNZS65yUc6FDKj-8dRRVHKHKz1udAri-Uewag130_assertion
a
np:Assertion
.
dgn-np:NP722047.RAVXrLuoBNZS65yUc6FDKj-8dRRVHKHKz1udAri-Uewag130_provenance
a
np:Provenance
.
dgn-np:NP722047.RAVXrLuoBNZS65yUc6FDKj-8dRRVHKHKz1udAri-Uewag130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP722047.RAVXrLuoBNZS65yUc6FDKj-8dRRVHKHKz1udAri-Uewag130_assertion
{
miriam-gene:410
a
ncit:C16612
.
lld:C0019247
a
ncit:C7057
.
dgn-gda:DGN5afb0f6f8b30eeb0c97d021380464992
sio:SIO_000628
miriam-gene:410
,
lld:C0019247
;
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sio:SIO_001121
.
}
dgn-np:NP722047.RAVXrLuoBNZS65yUc6FDKj-8dRRVHKHKz1udAri-Uewag130_provenance
{
dgn-np:NP722047.RAVXrLuoBNZS65yUc6FDKj-8dRRVHKHKz1udAri-Uewag130_assertion
dcterms:description
"[The general applicability of ASA makes this strategy universally useful for detection of specific mutations in the diagnostic analysis of genetic disease, and for typing of genetic polymorphisms or other sequence variations due to single-base differences.]. 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:8101084
;
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:NP722047.RAVXrLuoBNZS65yUc6FDKj-8dRRVHKHKz1udAri-Uewag130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:18+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
<
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> , <
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> , <
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
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dgn-void:disgenetrdf
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"v2.1.0" .
}