@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP643256.RAYjL2_KWcO3vHQ1ve7b79UhDFczUrkmqKg8tV4WlmbPk
> .
@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:NP643256.RAYjL2_KWcO3vHQ1ve7b79UhDFczUrkmqKg8tV4WlmbPk130_head
{
this:
np:hasAssertion
dgn-np:NP643256.RAYjL2_KWcO3vHQ1ve7b79UhDFczUrkmqKg8tV4WlmbPk130_assertion
;
np:hasProvenance
dgn-np:NP643256.RAYjL2_KWcO3vHQ1ve7b79UhDFczUrkmqKg8tV4WlmbPk130_provenance
;
np:hasPublicationInfo
dgn-np:NP643256.RAYjL2_KWcO3vHQ1ve7b79UhDFczUrkmqKg8tV4WlmbPk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP643256.RAYjL2_KWcO3vHQ1ve7b79UhDFczUrkmqKg8tV4WlmbPk130_assertion
a
np:Assertion
.
dgn-np:NP643256.RAYjL2_KWcO3vHQ1ve7b79UhDFczUrkmqKg8tV4WlmbPk130_provenance
a
np:Provenance
.
dgn-np:NP643256.RAYjL2_KWcO3vHQ1ve7b79UhDFczUrkmqKg8tV4WlmbPk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP643256.RAYjL2_KWcO3vHQ1ve7b79UhDFczUrkmqKg8tV4WlmbPk130_assertion
{
miriam-gene:1351
a
ncit:C16612
.
lld:C0016667
a
ncit:C7057
.
dgn-gda:DGN008ee3da2fa1e1a7363010a46c06f7dd
sio:SIO_000628
miriam-gene:1351
,
lld:C0016667
;
a
sio:SIO_001121
.
}
dgn-np:NP643256.RAYjL2_KWcO3vHQ1ve7b79UhDFczUrkmqKg8tV4WlmbPk130_provenance
{
dgn-np:NP643256.RAYjL2_KWcO3vHQ1ve7b79UhDFczUrkmqKg8tV4WlmbPk130_assertion
dcterms:description
"[Two DNA recombinant clones, shown by separate studies to contain DNA sequences homologous to the genes coding for the human blood coagulation Factors VIII and IX, were hybridized in situ to metaphases or prometaphases derived from patients with the fragile-X syndrome and from a normal control.]. 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:3924593
;
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:NP643256.RAYjL2_KWcO3vHQ1ve7b79UhDFczUrkmqKg8tV4WlmbPk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:27+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" .
}