Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP696783.RAyTHMqKHCT6lGQf_nH0V1wsBaLDz9uDC1NMMgNYa3PS4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP696783.RAyTHMqKHCT6lGQf_nH0V1wsBaLDz9uDC1NMMgNYa3PS4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP696783.RAyTHMqKHCT6lGQf_nH0V1wsBaLDz9uDC1NMMgNYa3PS4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP696783.RAyTHMqKHCT6lGQf_nH0V1wsBaLDz9uDC1NMMgNYa3PS4130_provenance.
- NP696783.RAyTHMqKHCT6lGQf_nH0V1wsBaLDz9uDC1NMMgNYa3PS4130_assertion description "[Different loss-of-function mutations were identified underlying PGRN haploinsufficiency in patients with frontotemporal lobar degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP696783.RAyTHMqKHCT6lGQf_nH0V1wsBaLDz9uDC1NMMgNYa3PS4130_provenance.
- NP696783.RAyTHMqKHCT6lGQf_nH0V1wsBaLDz9uDC1NMMgNYa3PS4130_assertion evidence source_evidence_literature NP696783.RAyTHMqKHCT6lGQf_nH0V1wsBaLDz9uDC1NMMgNYa3PS4130_provenance.
- NP696783.RAyTHMqKHCT6lGQf_nH0V1wsBaLDz9uDC1NMMgNYa3PS4130_assertion SIO_000772 18838661 NP696783.RAyTHMqKHCT6lGQf_nH0V1wsBaLDz9uDC1NMMgNYa3PS4130_provenance.
- NP696783.RAyTHMqKHCT6lGQf_nH0V1wsBaLDz9uDC1NMMgNYa3PS4130_assertion wasDerivedFrom befree-2016 NP696783.RAyTHMqKHCT6lGQf_nH0V1wsBaLDz9uDC1NMMgNYa3PS4130_provenance.
- NP696783.RAyTHMqKHCT6lGQf_nH0V1wsBaLDz9uDC1NMMgNYa3PS4130_assertion wasGeneratedBy ECO_0000203 NP696783.RAyTHMqKHCT6lGQf_nH0V1wsBaLDz9uDC1NMMgNYa3PS4130_provenance.
- befree-2016 importedOn "2016-02-19" NP696783.RAyTHMqKHCT6lGQf_nH0V1wsBaLDz9uDC1NMMgNYa3PS4130_provenance.