@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP475653.RAVowSMNI4vO4QvWQ5oeFuSzqNJLCnfILMkzrRQ_xMFaA
> .
@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:NP475653.RAVowSMNI4vO4QvWQ5oeFuSzqNJLCnfILMkzrRQ_xMFaA130_head
{
this:
np:hasAssertion
dgn-np:NP475653.RAVowSMNI4vO4QvWQ5oeFuSzqNJLCnfILMkzrRQ_xMFaA130_assertion
;
np:hasProvenance
dgn-np:NP475653.RAVowSMNI4vO4QvWQ5oeFuSzqNJLCnfILMkzrRQ_xMFaA130_provenance
;
np:hasPublicationInfo
dgn-np:NP475653.RAVowSMNI4vO4QvWQ5oeFuSzqNJLCnfILMkzrRQ_xMFaA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP475653.RAVowSMNI4vO4QvWQ5oeFuSzqNJLCnfILMkzrRQ_xMFaA130_assertion
a
np:Assertion
.
dgn-np:NP475653.RAVowSMNI4vO4QvWQ5oeFuSzqNJLCnfILMkzrRQ_xMFaA130_provenance
a
np:Provenance
.
dgn-np:NP475653.RAVowSMNI4vO4QvWQ5oeFuSzqNJLCnfILMkzrRQ_xMFaA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP475653.RAVowSMNI4vO4QvWQ5oeFuSzqNJLCnfILMkzrRQ_xMFaA130_assertion
{
miriam-gene:1741
a
ncit:C16612
.
lld:C0025362
a
ncit:C7057
.
dgn-gda:DGNab904bed490fca6c30aead7cb3480dcd
sio:SIO_000628
miriam-gene:1741
,
lld:C0025362
;
a
sio:SIO_001121
.
}
dgn-np:NP475653.RAVowSMNI4vO4QvWQ5oeFuSzqNJLCnfILMkzrRQ_xMFaA130_provenance
{
dgn-np:NP475653.RAVowSMNI4vO4QvWQ5oeFuSzqNJLCnfILMkzrRQ_xMFaA130_assertion
dcterms:description
"[Given that there are other eight MRX families overlapping this interval, none of them with known mutation, we conclude that at least one new gene responsible for nonsyndromic mental retardation is located in this 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:15526294
;
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:NP475653.RAVowSMNI4vO4QvWQ5oeFuSzqNJLCnfILMkzrRQ_xMFaA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:45+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" .
}