@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP819829.RAtrFRbYL-VQ7R4EkTwRWldrHtJHN-W-HM725sJynigdM
> .
@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:NP819829.RAtrFRbYL-VQ7R4EkTwRWldrHtJHN-W-HM725sJynigdM130_head
{
this:
np:hasAssertion
dgn-np:NP819829.RAtrFRbYL-VQ7R4EkTwRWldrHtJHN-W-HM725sJynigdM130_assertion
;
np:hasProvenance
dgn-np:NP819829.RAtrFRbYL-VQ7R4EkTwRWldrHtJHN-W-HM725sJynigdM130_provenance
;
np:hasPublicationInfo
dgn-np:NP819829.RAtrFRbYL-VQ7R4EkTwRWldrHtJHN-W-HM725sJynigdM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP819829.RAtrFRbYL-VQ7R4EkTwRWldrHtJHN-W-HM725sJynigdM130_assertion
a
np:Assertion
.
dgn-np:NP819829.RAtrFRbYL-VQ7R4EkTwRWldrHtJHN-W-HM725sJynigdM130_provenance
a
np:Provenance
.
dgn-np:NP819829.RAtrFRbYL-VQ7R4EkTwRWldrHtJHN-W-HM725sJynigdM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP819829.RAtrFRbYL-VQ7R4EkTwRWldrHtJHN-W-HM725sJynigdM130_assertion
{
miriam-gene:6035
a
ncit:C16612
.
lld:C0002736
a
ncit:C7057
.
dgn-gda:DGN5332cc7791573d00971e45e29d09e42a
sio:SIO_000628
miriam-gene:6035
,
lld:C0002736
;
a
sio:SIO_001121
.
}
dgn-np:NP819829.RAtrFRbYL-VQ7R4EkTwRWldrHtJHN-W-HM725sJynigdM130_provenance
{
dgn-np:NP819829.RAtrFRbYL-VQ7R4EkTwRWldrHtJHN-W-HM725sJynigdM130_assertion
dcterms:description
"[Interestingly, mutations in human angiogenin (hANG), a member of the ribonuclease A (RNase A) superfamily known to be involved in neovascularization, have been recently reported in patients with ALS, but the effects of these mutations on MN differentiation and survival has not been investigated.]. 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:17916583
;
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:NP819829.RAtrFRbYL-VQ7R4EkTwRWldrHtJHN-W-HM725sJynigdM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:22+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" .
}