@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1367716.RAo56Ialq_pDqhwi8aqGDmuE6aLoeaGr3fkVWWBok9CvE
> .
@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:NP1367716.RAo56Ialq_pDqhwi8aqGDmuE6aLoeaGr3fkVWWBok9CvE130_head
{
this:
np:hasAssertion
dgn-np:NP1367716.RAo56Ialq_pDqhwi8aqGDmuE6aLoeaGr3fkVWWBok9CvE130_assertion
;
np:hasProvenance
dgn-np:NP1367716.RAo56Ialq_pDqhwi8aqGDmuE6aLoeaGr3fkVWWBok9CvE130_provenance
;
np:hasPublicationInfo
dgn-np:NP1367716.RAo56Ialq_pDqhwi8aqGDmuE6aLoeaGr3fkVWWBok9CvE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1367716.RAo56Ialq_pDqhwi8aqGDmuE6aLoeaGr3fkVWWBok9CvE130_assertion
a
np:Assertion
.
dgn-np:NP1367716.RAo56Ialq_pDqhwi8aqGDmuE6aLoeaGr3fkVWWBok9CvE130_provenance
a
np:Provenance
.
dgn-np:NP1367716.RAo56Ialq_pDqhwi8aqGDmuE6aLoeaGr3fkVWWBok9CvE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1367716.RAo56Ialq_pDqhwi8aqGDmuE6aLoeaGr3fkVWWBok9CvE130_assertion
{
miriam-gene:3908
a
ncit:C16612
.
lld:C0699743
a
ncit:C7057
.
dgn-gda:DGN9006896ab93628f07931ef1769696243
sio:SIO_000628
miriam-gene:3908
,
lld:C0699743
;
a
sio:SIO_001121
.
}
dgn-np:NP1367716.RAo56Ialq_pDqhwi8aqGDmuE6aLoeaGr3fkVWWBok9CvE130_provenance
{
dgn-np:NP1367716.RAo56Ialq_pDqhwi8aqGDmuE6aLoeaGr3fkVWWBok9CvE130_assertion
dcterms:description
"[About half of the children with classical congenital muscular dystrophy (CMD) show an absence in their skeletal muscle of laminin alpha2 chain, one of the components of the extracellular matrix protein, merosin.]. 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:9039983
;
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:NP1367716.RAo56Ialq_pDqhwi8aqGDmuE6aLoeaGr3fkVWWBok9CvE130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:06+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" .
}