Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP607291.RAhZQTAhzuDeEl5uuSWlZeK2iB0tWIUeC6VP_PT3lkCw4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP607291.RAhZQTAhzuDeEl5uuSWlZeK2iB0tWIUeC6VP_PT3lkCw4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP607291.RAhZQTAhzuDeEl5uuSWlZeK2iB0tWIUeC6VP_PT3lkCw4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP607291.RAhZQTAhzuDeEl5uuSWlZeK2iB0tWIUeC6VP_PT3lkCw4130_provenance.
- NP607291.RAhZQTAhzuDeEl5uuSWlZeK2iB0tWIUeC6VP_PT3lkCw4130_assertion description "[Dyskeratosis congenita (DC) is an inherited bone marrow failure syndrome in which the known susceptibility genes (DKC1, TERC, and TERT) belong to the telomere maintenance pathway; patients with DC have very short telomeres.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP607291.RAhZQTAhzuDeEl5uuSWlZeK2iB0tWIUeC6VP_PT3lkCw4130_provenance.
- NP607291.RAhZQTAhzuDeEl5uuSWlZeK2iB0tWIUeC6VP_PT3lkCw4130_assertion evidence source_evidence_literature NP607291.RAhZQTAhzuDeEl5uuSWlZeK2iB0tWIUeC6VP_PT3lkCw4130_provenance.
- NP607291.RAhZQTAhzuDeEl5uuSWlZeK2iB0tWIUeC6VP_PT3lkCw4130_assertion SIO_000772 17468339 NP607291.RAhZQTAhzuDeEl5uuSWlZeK2iB0tWIUeC6VP_PT3lkCw4130_provenance.
- NP607291.RAhZQTAhzuDeEl5uuSWlZeK2iB0tWIUeC6VP_PT3lkCw4130_assertion wasDerivedFrom befree-2016 NP607291.RAhZQTAhzuDeEl5uuSWlZeK2iB0tWIUeC6VP_PT3lkCw4130_provenance.
- NP607291.RAhZQTAhzuDeEl5uuSWlZeK2iB0tWIUeC6VP_PT3lkCw4130_assertion wasGeneratedBy ECO_0000203 NP607291.RAhZQTAhzuDeEl5uuSWlZeK2iB0tWIUeC6VP_PT3lkCw4130_provenance.
- befree-2016 importedOn "2016-02-19" NP607291.RAhZQTAhzuDeEl5uuSWlZeK2iB0tWIUeC6VP_PT3lkCw4130_provenance.