@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP543826.RAovbYW6cQWMB-qWXw1yRVU8qYOnxBCoPICEm6J_ozHZ4
> .
@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:NP543826.RAovbYW6cQWMB-qWXw1yRVU8qYOnxBCoPICEm6J_ozHZ4130_head
{
this:
np:hasAssertion
dgn-np:NP543826.RAovbYW6cQWMB-qWXw1yRVU8qYOnxBCoPICEm6J_ozHZ4130_assertion
;
np:hasProvenance
dgn-np:NP543826.RAovbYW6cQWMB-qWXw1yRVU8qYOnxBCoPICEm6J_ozHZ4130_provenance
;
np:hasPublicationInfo
dgn-np:NP543826.RAovbYW6cQWMB-qWXw1yRVU8qYOnxBCoPICEm6J_ozHZ4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP543826.RAovbYW6cQWMB-qWXw1yRVU8qYOnxBCoPICEm6J_ozHZ4130_assertion
a
np:Assertion
.
dgn-np:NP543826.RAovbYW6cQWMB-qWXw1yRVU8qYOnxBCoPICEm6J_ozHZ4130_provenance
a
np:Provenance
.
dgn-np:NP543826.RAovbYW6cQWMB-qWXw1yRVU8qYOnxBCoPICEm6J_ozHZ4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP543826.RAovbYW6cQWMB-qWXw1yRVU8qYOnxBCoPICEm6J_ozHZ4130_assertion
{
miriam-gene:4359
a
ncit:C16612
.
lld:C0027888
a
ncit:C7057
.
dgn-gda:DGN632fc4e4cd366c95160a3677ca2e12ef
sio:SIO_000628
miriam-gene:4359
,
lld:C0027888
;
a
sio:SIO_001121
.
}
dgn-np:NP543826.RAovbYW6cQWMB-qWXw1yRVU8qYOnxBCoPICEm6J_ozHZ4130_provenance
{
dgn-np:NP543826.RAovbYW6cQWMB-qWXw1yRVU8qYOnxBCoPICEm6J_ozHZ4130_assertion
dcterms:description
"[We have restudied two clinically typical Charcot-Marie-Tooth neuropathy type 1 (CMT1; also known as hereditary motor and sensory neuropathy 1) pedigrees that were previously reported to be unlinked to the regions of proximal chromosome 1q and chromosome 17p by multipoint linkage analyses.]. 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:1407588
;
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:NP543826.RAovbYW6cQWMB-qWXw1yRVU8qYOnxBCoPICEm6J_ozHZ4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:28+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
<
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
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dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}