@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP533555.RAwqF9ufkQKnbRr82cdZWozN7QZ2z3a0XPEku4TQDDrcA
> .
@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/v3.0.0/void/
> .
dgn-np:NP533555.RAwqF9ufkQKnbRr82cdZWozN7QZ2z3a0XPEku4TQDDrcA130_head
{
this:
np:hasAssertion
dgn-np:NP533555.RAwqF9ufkQKnbRr82cdZWozN7QZ2z3a0XPEku4TQDDrcA130_assertion
;
np:hasProvenance
dgn-np:NP533555.RAwqF9ufkQKnbRr82cdZWozN7QZ2z3a0XPEku4TQDDrcA130_provenance
;
np:hasPublicationInfo
dgn-np:NP533555.RAwqF9ufkQKnbRr82cdZWozN7QZ2z3a0XPEku4TQDDrcA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP533555.RAwqF9ufkQKnbRr82cdZWozN7QZ2z3a0XPEku4TQDDrcA130_assertion
a
np:Assertion
.
dgn-np:NP533555.RAwqF9ufkQKnbRr82cdZWozN7QZ2z3a0XPEku4TQDDrcA130_provenance
a
np:Provenance
.
dgn-np:NP533555.RAwqF9ufkQKnbRr82cdZWozN7QZ2z3a0XPEku4TQDDrcA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP533555.RAwqF9ufkQKnbRr82cdZWozN7QZ2z3a0XPEku4TQDDrcA130_assertion
{
miriam-gene:3949
a
ncit:C16612
.
lld:C0342880
a
ncit:C7057
.
dgn-gda:DGN2bf4d74efaf9969c2503ba0162bb98c4
sio:SIO_000628
miriam-gene:3949
,
lld:C0342880
;
a
sio:SIO_001121
.
}
dgn-np:NP533555.RAwqF9ufkQKnbRr82cdZWozN7QZ2z3a0XPEku4TQDDrcA130_provenance
{
dgn-np:NP533555.RAwqF9ufkQKnbRr82cdZWozN7QZ2z3a0XPEku4TQDDrcA130_assertion
dcterms:description
"[The ability to identify mutant LDL receptor genes for prenatal diagnosis of homozygous FH or to study the role of the LDL receptor gene in polygenic hypercholesterolemia requires the use of closely linked RFLPs.]. 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:2563635
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP533555.RAwqF9ufkQKnbRr82cdZWozN7QZ2z3a0XPEku4TQDDrcA130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:42:55+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}