@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP879944.RAzZiYctBV2PLOiEMWWYEZOmVWL9miCSDhrKUZxoxQBhw
> .
@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:NP879944.RAzZiYctBV2PLOiEMWWYEZOmVWL9miCSDhrKUZxoxQBhw130_head
{
this:
np:hasAssertion
dgn-np:NP879944.RAzZiYctBV2PLOiEMWWYEZOmVWL9miCSDhrKUZxoxQBhw130_assertion
;
np:hasProvenance
dgn-np:NP879944.RAzZiYctBV2PLOiEMWWYEZOmVWL9miCSDhrKUZxoxQBhw130_provenance
;
np:hasPublicationInfo
dgn-np:NP879944.RAzZiYctBV2PLOiEMWWYEZOmVWL9miCSDhrKUZxoxQBhw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP879944.RAzZiYctBV2PLOiEMWWYEZOmVWL9miCSDhrKUZxoxQBhw130_assertion
a
np:Assertion
.
dgn-np:NP879944.RAzZiYctBV2PLOiEMWWYEZOmVWL9miCSDhrKUZxoxQBhw130_provenance
a
np:Provenance
.
dgn-np:NP879944.RAzZiYctBV2PLOiEMWWYEZOmVWL9miCSDhrKUZxoxQBhw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP879944.RAzZiYctBV2PLOiEMWWYEZOmVWL9miCSDhrKUZxoxQBhw130_assertion
{
miriam-gene:7291
a
ncit:C16612
.
lld:C0025362
a
ncit:C7057
.
dgn-gda:DGN82b1e60912d9767fe852d663961a01f7
sio:SIO_000628
miriam-gene:7291
,
lld:C0025362
;
a
sio:SIO_001121
.
}
dgn-np:NP879944.RAzZiYctBV2PLOiEMWWYEZOmVWL9miCSDhrKUZxoxQBhw130_provenance
{
dgn-np:NP879944.RAzZiYctBV2PLOiEMWWYEZOmVWL9miCSDhrKUZxoxQBhw130_assertion
dcterms:description
"[These data definitively implicate perturbation of TGFbeta signaling in many common human phenotypes, including craniosynostosis, cleft palate, arterial aneurysms, congenital heart disease and mental retardation, and suggest that comprehensive mechanistic insight will require consideration of both primary and compensatory events.]. 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:15731757
;
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:NP879944.RAzZiYctBV2PLOiEMWWYEZOmVWL9miCSDhrKUZxoxQBhw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:57+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" .
}