@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP54327.RAAo09p0zZrLFzUmdl7tL86jnWaWuK0i2nYYUc9aEFCbo
> .
@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:NP54327.RAAo09p0zZrLFzUmdl7tL86jnWaWuK0i2nYYUc9aEFCbo130_head
{
this:
np:hasAssertion
dgn-np:NP54327.RAAo09p0zZrLFzUmdl7tL86jnWaWuK0i2nYYUc9aEFCbo130_assertion
;
np:hasProvenance
dgn-np:NP54327.RAAo09p0zZrLFzUmdl7tL86jnWaWuK0i2nYYUc9aEFCbo130_provenance
;
np:hasPublicationInfo
dgn-np:NP54327.RAAo09p0zZrLFzUmdl7tL86jnWaWuK0i2nYYUc9aEFCbo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP54327.RAAo09p0zZrLFzUmdl7tL86jnWaWuK0i2nYYUc9aEFCbo130_assertion
a
np:Assertion
.
dgn-np:NP54327.RAAo09p0zZrLFzUmdl7tL86jnWaWuK0i2nYYUc9aEFCbo130_provenance
a
np:Provenance
.
dgn-np:NP54327.RAAo09p0zZrLFzUmdl7tL86jnWaWuK0i2nYYUc9aEFCbo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP54327.RAAo09p0zZrLFzUmdl7tL86jnWaWuK0i2nYYUc9aEFCbo130_assertion
{
miriam-gene:4360
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGN70a37718e27896e529d11cdc553a0066
sio:SIO_000628
miriam-gene:4360
,
lld:C1527249
;
a
sio:SIO_001122
.
}
dgn-np:NP54327.RAAo09p0zZrLFzUmdl7tL86jnWaWuK0i2nYYUc9aEFCbo130_provenance
{
dgn-np:NP54327.RAAo09p0zZrLFzUmdl7tL86jnWaWuK0i2nYYUc9aEFCbo130_assertion
dcterms:description
"[The identification of this MSH2 founder mutation has important implications for the design of mutation-detection strategies for the southern Chinese population. Since there were major emigrations from Hong Kong and Guangdong province during the 19th and 20th centuries, this finding is also significant for Chinese communities worldwide.]. 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:15042510
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP54327.RAAo09p0zZrLFzUmdl7tL86jnWaWuK0i2nYYUc9aEFCbo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:25+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
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
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
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}