Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP431322.RA1RAbkNNgjxCAl1tFSlVdWBIzEfW5Ec13UKrlBszB1v4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP431322.RA1RAbkNNgjxCAl1tFSlVdWBIzEfW5Ec13UKrlBszB1v4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP431322.RA1RAbkNNgjxCAl1tFSlVdWBIzEfW5Ec13UKrlBszB1v4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP431322.RA1RAbkNNgjxCAl1tFSlVdWBIzEfW5Ec13UKrlBszB1v4130_provenance.
- NP431322.RA1RAbkNNgjxCAl1tFSlVdWBIzEfW5Ec13UKrlBszB1v4130_assertion description "[To investigate the progression of cognitive impairment and its behavioral aspects in patients with SPG4-linked autosomal dominant hereditary spastic paraplegia (SPG4-ADHSP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP431322.RA1RAbkNNgjxCAl1tFSlVdWBIzEfW5Ec13UKrlBszB1v4130_provenance.
- NP431322.RA1RAbkNNgjxCAl1tFSlVdWBIzEfW5Ec13UKrlBszB1v4130_assertion evidence source_evidence_literature NP431322.RA1RAbkNNgjxCAl1tFSlVdWBIzEfW5Ec13UKrlBszB1v4130_provenance.
- NP431322.RA1RAbkNNgjxCAl1tFSlVdWBIzEfW5Ec13UKrlBszB1v4130_assertion SIO_000772 14872021 NP431322.RA1RAbkNNgjxCAl1tFSlVdWBIzEfW5Ec13UKrlBszB1v4130_provenance.
- NP431322.RA1RAbkNNgjxCAl1tFSlVdWBIzEfW5Ec13UKrlBszB1v4130_assertion wasDerivedFrom befree-2016 NP431322.RA1RAbkNNgjxCAl1tFSlVdWBIzEfW5Ec13UKrlBszB1v4130_provenance.
- NP431322.RA1RAbkNNgjxCAl1tFSlVdWBIzEfW5Ec13UKrlBszB1v4130_assertion wasGeneratedBy ECO_0000203 NP431322.RA1RAbkNNgjxCAl1tFSlVdWBIzEfW5Ec13UKrlBszB1v4130_provenance.
- befree-2016 importedOn "2016-02-19" NP431322.RA1RAbkNNgjxCAl1tFSlVdWBIzEfW5Ec13UKrlBszB1v4130_provenance.