@prefix dc: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP807292.RAFMRxJhT4UWRqdAhdd_-Q2QPAn8AkK-GeuhnGObXnvJg
> .
@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 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:NP807292.RAFMRxJhT4UWRqdAhdd_-Q2QPAn8AkK-GeuhnGObXnvJg130_head
{
this:
np:hasAssertion
dgn-np:NP807292.RAFMRxJhT4UWRqdAhdd_-Q2QPAn8AkK-GeuhnGObXnvJg130_assertion
;
np:hasProvenance
dgn-np:NP807292.RAFMRxJhT4UWRqdAhdd_-Q2QPAn8AkK-GeuhnGObXnvJg130_provenance
;
np:hasPublicationInfo
dgn-np:NP807292.RAFMRxJhT4UWRqdAhdd_-Q2QPAn8AkK-GeuhnGObXnvJg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP807292.RAFMRxJhT4UWRqdAhdd_-Q2QPAn8AkK-GeuhnGObXnvJg130_assertion
a
np:Assertion
.
dgn-np:NP807292.RAFMRxJhT4UWRqdAhdd_-Q2QPAn8AkK-GeuhnGObXnvJg130_provenance
a
np:Provenance
.
dgn-np:NP807292.RAFMRxJhT4UWRqdAhdd_-Q2QPAn8AkK-GeuhnGObXnvJg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP807292.RAFMRxJhT4UWRqdAhdd_-Q2QPAn8AkK-GeuhnGObXnvJg130_assertion
{
miriam-gene:6576
a
ncit:C16612
.
lld:C0025267
a
ncit:C7057
.
dgn-gda:DGN0469c2d09cb23c9a5f290679e02d217c
sio:SIO_000628
miriam-gene:6576
,
lld:C0025267
;
a
sio:SIO_001121
.
}
dgn-np:NP807292.RAFMRxJhT4UWRqdAhdd_-Q2QPAn8AkK-GeuhnGObXnvJg130_provenance
{
dgn-np:NP807292.RAFMRxJhT4UWRqdAhdd_-Q2QPAn8AkK-GeuhnGObXnvJg130_assertion
dc:description
"[We allelotyped 33 affected individuals from an extensive MEN1 kindred using eight polymorphic markers located on chromosome 11q13, including two new markers (D11S4907 and D11S4908) that we derived and mapped to the SEA-D11S913 region.]. 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:9067266
;
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:NP807292.RAFMRxJhT4UWRqdAhdd_-Q2QPAn8AkK-GeuhnGObXnvJg130_publicationInfo
{
this:
dc:created
"2014-10-02T12:40:15+02:00"^^
xsd:dateTime
;
dc:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dc:rightsHolder
dgn-void:IBIGroup
;
dc:subject
sio: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" .
}