@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP830571.RA0hYL1Is3lQrmemDIqRNzUCc1BaVi-YRbT0Vgc5Olhqs
> .
@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:NP830571.RA0hYL1Is3lQrmemDIqRNzUCc1BaVi-YRbT0Vgc5Olhqs130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP830571.RA0hYL1Is3lQrmemDIqRNzUCc1BaVi-YRbT0Vgc5Olhqs130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP830571.RA0hYL1Is3lQrmemDIqRNzUCc1BaVi-YRbT0Vgc5Olhqs130_assertion
a
np:Assertion
.
dgn-np:NP830571.RA0hYL1Is3lQrmemDIqRNzUCc1BaVi-YRbT0Vgc5Olhqs130_provenance
a
np:Provenance
.
dgn-np:NP830571.RA0hYL1Is3lQrmemDIqRNzUCc1BaVi-YRbT0Vgc5Olhqs130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:7535
a
ncit:C16612
.
lld:C0017638
a
ncit:C7057
.
dgn-gda:DGN335fd12593068a8ee00ade15092d0a07
sio:SIO_000628
miriam-gene:7535
,
lld:C0017638
;
a
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.
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dgn-np:NP830571.RA0hYL1Is3lQrmemDIqRNzUCc1BaVi-YRbT0Vgc5Olhqs130_provenance
{
dgn-np:NP830571.RA0hYL1Is3lQrmemDIqRNzUCc1BaVi-YRbT0Vgc5Olhqs130_assertion
dcterms:description
"[In addition, we have developed three new polymorphic microsatellite markers (D19S1180, D19S1181, and D19S1182) that map between D19S412 and STD and have used these new markers to identify two gliomas with small deletions between the D19S412 and STD markers.]. 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:10918389
;
prov:wasDerivedFrom
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;
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:NP830571.RA0hYL1Is3lQrmemDIqRNzUCc1BaVi-YRbT0Vgc5Olhqs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:28+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
> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
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"v2.1.0" .
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