@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP318233.RA86hAHFsSeVTE1AQxLKBDqPkN3CYKuWcs0vW-76W4-DE
> .
@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:NP318233.RA86hAHFsSeVTE1AQxLKBDqPkN3CYKuWcs0vW-76W4-DE130_head
{
this:
np:hasAssertion
dgn-np:NP318233.RA86hAHFsSeVTE1AQxLKBDqPkN3CYKuWcs0vW-76W4-DE130_assertion
;
np:hasProvenance
dgn-np:NP318233.RA86hAHFsSeVTE1AQxLKBDqPkN3CYKuWcs0vW-76W4-DE130_provenance
;
np:hasPublicationInfo
dgn-np:NP318233.RA86hAHFsSeVTE1AQxLKBDqPkN3CYKuWcs0vW-76W4-DE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP318233.RA86hAHFsSeVTE1AQxLKBDqPkN3CYKuWcs0vW-76W4-DE130_assertion
a
np:Assertion
.
dgn-np:NP318233.RA86hAHFsSeVTE1AQxLKBDqPkN3CYKuWcs0vW-76W4-DE130_provenance
a
np:Provenance
.
dgn-np:NP318233.RA86hAHFsSeVTE1AQxLKBDqPkN3CYKuWcs0vW-76W4-DE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP318233.RA86hAHFsSeVTE1AQxLKBDqPkN3CYKuWcs0vW-76W4-DE130_assertion
{
miriam-gene:94
a
ncit:C16612
.
lld:C1838163
a
ncit:C7057
.
dgn-gda:DGN8ba8c98d6b9f85ee96548d621068ebb4
sio:SIO_000628
miriam-gene:94
,
lld:C1838163
;
a
sio:SIO_001121
.
}
dgn-np:NP318233.RA86hAHFsSeVTE1AQxLKBDqPkN3CYKuWcs0vW-76W4-DE130_provenance
{
dgn-np:NP318233.RA86hAHFsSeVTE1AQxLKBDqPkN3CYKuWcs0vW-76W4-DE130_assertion
dcterms:description
"[This study gives a preliminary insight into the potential structure of ALK1(EC) and into the structural effects of HHT2 associated mutations, which can be useful to predict the potential effect of each single mutation, to devise new biological experiments and to interpret the biological significance of new mutations, private mutations, or non-synonymous polymorphisms.]. 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:22028876
;
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:NP318233.RA86hAHFsSeVTE1AQxLKBDqPkN3CYKuWcs0vW-76W4-DE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:04+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" .
}