@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP248350.RAbOV71R9ajiSWkZcYEEMo0K9WYRcBH5JhwnyQz4-NVnw
> .
@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:NP248350.RAbOV71R9ajiSWkZcYEEMo0K9WYRcBH5JhwnyQz4-NVnw130_head
{
this:
np:hasAssertion
dgn-np:NP248350.RAbOV71R9ajiSWkZcYEEMo0K9WYRcBH5JhwnyQz4-NVnw130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP248350.RAbOV71R9ajiSWkZcYEEMo0K9WYRcBH5JhwnyQz4-NVnw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP248350.RAbOV71R9ajiSWkZcYEEMo0K9WYRcBH5JhwnyQz4-NVnw130_assertion
a
np:Assertion
.
dgn-np:NP248350.RAbOV71R9ajiSWkZcYEEMo0K9WYRcBH5JhwnyQz4-NVnw130_provenance
a
np:Provenance
.
dgn-np:NP248350.RAbOV71R9ajiSWkZcYEEMo0K9WYRcBH5JhwnyQz4-NVnw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP248350.RAbOV71R9ajiSWkZcYEEMo0K9WYRcBH5JhwnyQz4-NVnw130_assertion
{
miriam-gene:3949
a
ncit:C16612
.
lld:C0020445
a
ncit:C7057
.
dgn-gda:DGNe7974a3ccb3e89d936e69d6773055c13
sio:SIO_000628
miriam-gene:3949
,
lld:C0020445
;
a
sio:SIO_001121
.
}
dgn-np:NP248350.RAbOV71R9ajiSWkZcYEEMo0K9WYRcBH5JhwnyQz4-NVnw130_provenance
{
dgn-np:NP248350.RAbOV71R9ajiSWkZcYEEMo0K9WYRcBH5JhwnyQz4-NVnw130_assertion
dcterms:description
"[In order to obtain a survey of the mutations being prevalent in Northern Germany and to enable molecular genetic testing for families with clinically diagnosed familial hypercholesterolemia (FH), we screened 46 unrelated German individuals with elevated LDL levels for mutations in the 18 exons and their flanking intron sequences including the promotor region of the LDL receptor (LDLR) gene.]. 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:10090484
;
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:NP248350.RAbOV71R9ajiSWkZcYEEMo0K9WYRcBH5JhwnyQz4-NVnw130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:38+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
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;
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" .
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pav:version
"v4.0.0" .
}