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http://rdf.disgenet.org/nanopublications.trig#NP869215.RAYEioD9W5NxvsaIP6ReXdB_7qO4ZHxymzGlqsWOJJXRA
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP869215.RAYEioD9W5NxvsaIP6ReXdB_7qO4ZHxymzGlqsWOJJXRA130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP869215.RAYEioD9W5NxvsaIP6ReXdB_7qO4ZHxymzGlqsWOJJXRA130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP869215.RAYEioD9W5NxvsaIP6ReXdB_7qO4ZHxymzGlqsWOJJXRA130_assertion
a
np:Assertion
.
dgn-np:NP869215.RAYEioD9W5NxvsaIP6ReXdB_7qO4ZHxymzGlqsWOJJXRA130_provenance
a
np:Provenance
.
dgn-np:NP869215.RAYEioD9W5NxvsaIP6ReXdB_7qO4ZHxymzGlqsWOJJXRA130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:4296
a
ncit:C16612
.
lld:C1333600
a
ncit:C7057
.
dgn-gda:DGN33ace3924243cd77d9c975f609f38a71
sio:SIO_000628
miriam-gene:4296
,
lld:C1333600
;
a
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.
}
dgn-np:NP869215.RAYEioD9W5NxvsaIP6ReXdB_7qO4ZHxymzGlqsWOJJXRA130_provenance
{
dgn-np:NP869215.RAYEioD9W5NxvsaIP6ReXdB_7qO4ZHxymzGlqsWOJJXRA130_assertion
dcterms:description
"[Since the MEN1 susceptibility locus is also located within the 11q13.1 region, we have carried out Southern and Northern blot analyses, as well as protein truncation assays to establish whether abnormalities in MLK-3 lead to the development of this familial cancer syndrome.]. 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:9187672
;
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 .
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dgn-np:NP869215.RAYEioD9W5NxvsaIP6ReXdB_7qO4ZHxymzGlqsWOJJXRA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:51+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
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pav:authoredBy
<
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> , <
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> , <
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> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
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