@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP92137.RAY6cwy1SHpHjAevi9FZLNK7ZV8vCDcxfJuaA5i0yqBjQ
> .
@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:NP92137.RAY6cwy1SHpHjAevi9FZLNK7ZV8vCDcxfJuaA5i0yqBjQ130_head
{
this:
np:hasAssertion
dgn-np:NP92137.RAY6cwy1SHpHjAevi9FZLNK7ZV8vCDcxfJuaA5i0yqBjQ130_assertion
;
np:hasProvenance
dgn-np:NP92137.RAY6cwy1SHpHjAevi9FZLNK7ZV8vCDcxfJuaA5i0yqBjQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP92137.RAY6cwy1SHpHjAevi9FZLNK7ZV8vCDcxfJuaA5i0yqBjQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP92137.RAY6cwy1SHpHjAevi9FZLNK7ZV8vCDcxfJuaA5i0yqBjQ130_assertion
a
np:Assertion
.
dgn-np:NP92137.RAY6cwy1SHpHjAevi9FZLNK7ZV8vCDcxfJuaA5i0yqBjQ130_provenance
a
np:Provenance
.
dgn-np:NP92137.RAY6cwy1SHpHjAevi9FZLNK7ZV8vCDcxfJuaA5i0yqBjQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP92137.RAY6cwy1SHpHjAevi9FZLNK7ZV8vCDcxfJuaA5i0yqBjQ130_assertion
{
miriam-gene:6692
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGNfdf83916ce5e80ae302db85c16677553
sio:SIO_000628
miriam-gene:6692
,
lld:C0006142
;
a
sio:SIO_001122
.
}
dgn-np:NP92137.RAY6cwy1SHpHjAevi9FZLNK7ZV8vCDcxfJuaA5i0yqBjQ130_provenance
{
dgn-np:NP92137.RAY6cwy1SHpHjAevi9FZLNK7ZV8vCDcxfJuaA5i0yqBjQ130_assertion
dcterms:description
"[This is the first study showing that genetic variation in matriptase has clinical importance. The results encourage further study on the genetic variation affecting protein levels and function in type II transmembrane serine proteases.]. 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:20716618
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP92137.RAY6cwy1SHpHjAevi9FZLNK7ZV8vCDcxfJuaA5i0yqBjQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:45+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" .
}