@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP296118.RApmkZox8-RqCSdkQgczgfVrSjxs-huWncfAy6rlz1dHw
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP296118.RApmkZox8-RqCSdkQgczgfVrSjxs-huWncfAy6rlz1dHw130_head
{
this:
np:hasAssertion
dgn-np:NP296118.RApmkZox8-RqCSdkQgczgfVrSjxs-huWncfAy6rlz1dHw130_assertion
;
np:hasProvenance
dgn-np:NP296118.RApmkZox8-RqCSdkQgczgfVrSjxs-huWncfAy6rlz1dHw130_provenance
;
np:hasPublicationInfo
dgn-np:NP296118.RApmkZox8-RqCSdkQgczgfVrSjxs-huWncfAy6rlz1dHw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP296118.RApmkZox8-RqCSdkQgczgfVrSjxs-huWncfAy6rlz1dHw130_assertion
a
np:Assertion
.
dgn-np:NP296118.RApmkZox8-RqCSdkQgczgfVrSjxs-huWncfAy6rlz1dHw130_provenance
a
np:Provenance
.
dgn-np:NP296118.RApmkZox8-RqCSdkQgczgfVrSjxs-huWncfAy6rlz1dHw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP296118.RApmkZox8-RqCSdkQgczgfVrSjxs-huWncfAy6rlz1dHw130_assertion
{
miriam-gene:1756
a
ncit:C16612
.
lld:C0013264
a
ncit:C7057
.
dgn-gda:DGNf18364eef7eb0607bf63f02c3223f2b9
sio:SIO_000628
miriam-gene:1756
,
lld:C0013264
;
a
sio:SIO_001121
.
}
dgn-np:NP296118.RApmkZox8-RqCSdkQgczgfVrSjxs-huWncfAy6rlz1dHw130_provenance
{
dgn-np:NP296118.RApmkZox8-RqCSdkQgczgfVrSjxs-huWncfAy6rlz1dHw130_assertion
dcterms:description
"[Since the identification of dystrophin as the causative factor in Duchenne muscular dystrophy, an increasing amount of information on the molecular basis of muscular dystrophies has facilitated the division of these heterogeneous disorders into distinct groups.]. 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:11005802
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP296118.RApmkZox8-RqCSdkQgczgfVrSjxs-huWncfAy6rlz1dHw130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:00+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}