Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP426307.RA_1q4UZAPyMZ3l9K_Ob9jVQSSIs5cPfxJdEW_cLZTYU4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP426307.RA_1q4UZAPyMZ3l9K_Ob9jVQSSIs5cPfxJdEW_cLZTYU4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP426307.RA_1q4UZAPyMZ3l9K_Ob9jVQSSIs5cPfxJdEW_cLZTYU4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP426307.RA_1q4UZAPyMZ3l9K_Ob9jVQSSIs5cPfxJdEW_cLZTYU4130_provenance.
- NP426307.RA_1q4UZAPyMZ3l9K_Ob9jVQSSIs5cPfxJdEW_cLZTYU4130_assertion description "[Novel mutations in the Atlastin gene (SPG3A) in families with autosomal dominant hereditary spastic paraplegia and evidence for late onset forms of HSP linked to the SPG3A locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP426307.RA_1q4UZAPyMZ3l9K_Ob9jVQSSIs5cPfxJdEW_cLZTYU4130_provenance.
- NP426307.RA_1q4UZAPyMZ3l9K_Ob9jVQSSIs5cPfxJdEW_cLZTYU4130_assertion evidence source_evidence_literature NP426307.RA_1q4UZAPyMZ3l9K_Ob9jVQSSIs5cPfxJdEW_cLZTYU4130_provenance.
- NP426307.RA_1q4UZAPyMZ3l9K_Ob9jVQSSIs5cPfxJdEW_cLZTYU4130_assertion SIO_000772 14695538 NP426307.RA_1q4UZAPyMZ3l9K_Ob9jVQSSIs5cPfxJdEW_cLZTYU4130_provenance.
- NP426307.RA_1q4UZAPyMZ3l9K_Ob9jVQSSIs5cPfxJdEW_cLZTYU4130_assertion wasDerivedFrom befree-2016 NP426307.RA_1q4UZAPyMZ3l9K_Ob9jVQSSIs5cPfxJdEW_cLZTYU4130_provenance.
- NP426307.RA_1q4UZAPyMZ3l9K_Ob9jVQSSIs5cPfxJdEW_cLZTYU4130_assertion wasGeneratedBy ECO_0000203 NP426307.RA_1q4UZAPyMZ3l9K_Ob9jVQSSIs5cPfxJdEW_cLZTYU4130_provenance.
- befree-2016 importedOn "2016-02-19" NP426307.RA_1q4UZAPyMZ3l9K_Ob9jVQSSIs5cPfxJdEW_cLZTYU4130_provenance.