@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP361794.RAWSw8JgeOHIXcIpOGP1CuAR5bE19bK6Uz2VnK_U8ILS8
> .
@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:NP361794.RAWSw8JgeOHIXcIpOGP1CuAR5bE19bK6Uz2VnK_U8ILS8130_head
{
this:
np:hasAssertion
dgn-np:NP361794.RAWSw8JgeOHIXcIpOGP1CuAR5bE19bK6Uz2VnK_U8ILS8130_assertion
;
np:hasProvenance
dgn-np:NP361794.RAWSw8JgeOHIXcIpOGP1CuAR5bE19bK6Uz2VnK_U8ILS8130_provenance
;
np:hasPublicationInfo
dgn-np:NP361794.RAWSw8JgeOHIXcIpOGP1CuAR5bE19bK6Uz2VnK_U8ILS8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP361794.RAWSw8JgeOHIXcIpOGP1CuAR5bE19bK6Uz2VnK_U8ILS8130_assertion
a
np:Assertion
.
dgn-np:NP361794.RAWSw8JgeOHIXcIpOGP1CuAR5bE19bK6Uz2VnK_U8ILS8130_provenance
a
np:Provenance
.
dgn-np:NP361794.RAWSw8JgeOHIXcIpOGP1CuAR5bE19bK6Uz2VnK_U8ILS8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP361794.RAWSw8JgeOHIXcIpOGP1CuAR5bE19bK6Uz2VnK_U8ILS8130_assertion
{
miriam-gene:4088
a
ncit:C16612
.
lld:C3151087
a
ncit:C7057
.
dgn-gda:DGN9a02c251f6183c844a8adf1a6c535db5
sio:SIO_000628
miriam-gene:4088
,
lld:C3151087
;
a
sio:SIO_001121
.
}
dgn-np:NP361794.RAWSw8JgeOHIXcIpOGP1CuAR5bE19bK6Uz2VnK_U8ILS8130_provenance
{
dgn-np:NP361794.RAWSw8JgeOHIXcIpOGP1CuAR5bE19bK6Uz2VnK_U8ILS8130_assertion
dcterms:description
"[SMAD3 mutations were recently described in patients with aneurysms osteoarthritis syndrome and some of the features of this syndrome were identified in individuals in our cohort, but these features were notably absent in many SMAD3 mutation carriers.]. 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:21778426
;
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:NP361794.RAWSw8JgeOHIXcIpOGP1CuAR5bE19bK6Uz2VnK_U8ILS8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:32+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" .
}