@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP402998.RAH-1KVzr4nyasjSuuFFT_ZhkFGynCesKUmhVF-6eOhEg
> .
@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/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@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/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP402998.RAH-1KVzr4nyasjSuuFFT_ZhkFGynCesKUmhVF-6eOhEg130_head
{
this:
np:hasAssertion
dgn-np:NP402998.RAH-1KVzr4nyasjSuuFFT_ZhkFGynCesKUmhVF-6eOhEg130_assertion
;
np:hasProvenance
dgn-np:NP402998.RAH-1KVzr4nyasjSuuFFT_ZhkFGynCesKUmhVF-6eOhEg130_provenance
;
np:hasPublicationInfo
dgn-np:NP402998.RAH-1KVzr4nyasjSuuFFT_ZhkFGynCesKUmhVF-6eOhEg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP402998.RAH-1KVzr4nyasjSuuFFT_ZhkFGynCesKUmhVF-6eOhEg130_assertion
a
np:Assertion
.
dgn-np:NP402998.RAH-1KVzr4nyasjSuuFFT_ZhkFGynCesKUmhVF-6eOhEg130_provenance
a
np:Provenance
.
dgn-np:NP402998.RAH-1KVzr4nyasjSuuFFT_ZhkFGynCesKUmhVF-6eOhEg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP402998.RAH-1KVzr4nyasjSuuFFT_ZhkFGynCesKUmhVF-6eOhEg130_assertion
{
miriam-gene:10855
a
ncit:C16612
.
lld:C0018133
a
ncit:C7057
.
dgn-gda:DGNa26f03705b73ecd3b1c6ff24120e56f6
sio:SIO_000628
miriam-gene:10855
,
lld:C0018133
;
a
sio:SIO_001121
.
}
dgn-np:NP402998.RAH-1KVzr4nyasjSuuFFT_ZhkFGynCesKUmhVF-6eOhEg130_provenance
{
dgn-np:NP402998.RAH-1KVzr4nyasjSuuFFT_ZhkFGynCesKUmhVF-6eOhEg130_assertion
dcterms:description
"[Identification and characterization of a human heparanase splice variant (T5) devoid of enzymatic activity and endowed with protumorigenic characteristics, elucidation of cross-talk between heparanase and other extracellular matrix-degrading enzymes, and identification of single nucleotide polymorphism associated with heparanase expression and increased risk of graft versus host disease add other layers of complexity to heparanase function in health and disease.]. 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:20840586
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP402998.RAH-1KVzr4nyasjSuuFFT_ZhkFGynCesKUmhVF-6eOhEg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:00+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:disgenetrdf
;
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
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}