@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP776313.RAjIDfgBkhQrDrObcFAVNoqvTfkQ2CwNtf4VC7MSMmoP8
> .
@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:NP776313.RAjIDfgBkhQrDrObcFAVNoqvTfkQ2CwNtf4VC7MSMmoP8130_head
{
this:
np:hasAssertion
dgn-np:NP776313.RAjIDfgBkhQrDrObcFAVNoqvTfkQ2CwNtf4VC7MSMmoP8130_assertion
;
np:hasProvenance
dgn-np:NP776313.RAjIDfgBkhQrDrObcFAVNoqvTfkQ2CwNtf4VC7MSMmoP8130_provenance
;
np:hasPublicationInfo
dgn-np:NP776313.RAjIDfgBkhQrDrObcFAVNoqvTfkQ2CwNtf4VC7MSMmoP8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP776313.RAjIDfgBkhQrDrObcFAVNoqvTfkQ2CwNtf4VC7MSMmoP8130_assertion
a
np:Assertion
.
dgn-np:NP776313.RAjIDfgBkhQrDrObcFAVNoqvTfkQ2CwNtf4VC7MSMmoP8130_provenance
a
np:Provenance
.
dgn-np:NP776313.RAjIDfgBkhQrDrObcFAVNoqvTfkQ2CwNtf4VC7MSMmoP8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP776313.RAjIDfgBkhQrDrObcFAVNoqvTfkQ2CwNtf4VC7MSMmoP8130_assertion
{
miriam-gene:7450
a
ncit:C16612
.
lld:C1264040
a
ncit:C7057
.
dgn-gda:DGN817b578a3ec94d39260950ad63be27af
sio:SIO_000628
miriam-gene:7450
,
lld:C1264040
;
a
sio:SIO_001121
.
}
dgn-np:NP776313.RAjIDfgBkhQrDrObcFAVNoqvTfkQ2CwNtf4VC7MSMmoP8130_provenance
{
dgn-np:NP776313.RAjIDfgBkhQrDrObcFAVNoqvTfkQ2CwNtf4VC7MSMmoP8130_assertion
dcterms:description
"[Additional resources include references linked to sequence variation entries, descriptors of each VWD type, genomic and cDNA sequences, nomenclature for VWF and its attributes, Human Genome Variation Society sequence variant nomenclature recommendations, multimer images, and related densitometry traces for type 2 VWD.]. 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:22102189
;
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:NP776313.RAjIDfgBkhQrDrObcFAVNoqvTfkQ2CwNtf4VC7MSMmoP8130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:45:29+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" .
}