Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP742988.RA9mqeWn0NXH1DASeEQrB0m-0XvjshAYghwZzf8kctDNo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP742988.RA9mqeWn0NXH1DASeEQrB0m-0XvjshAYghwZzf8kctDNo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP742988.RA9mqeWn0NXH1DASeEQrB0m-0XvjshAYghwZzf8kctDNo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP742988.RA9mqeWn0NXH1DASeEQrB0m-0XvjshAYghwZzf8kctDNo130_provenance.
- NP742988.RA9mqeWn0NXH1DASeEQrB0m-0XvjshAYghwZzf8kctDNo130_assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP742988.RA9mqeWn0NXH1DASeEQrB0m-0XvjshAYghwZzf8kctDNo130_provenance.
- NP742988.RA9mqeWn0NXH1DASeEQrB0m-0XvjshAYghwZzf8kctDNo130_assertion evidence source_evidence_literature NP742988.RA9mqeWn0NXH1DASeEQrB0m-0XvjshAYghwZzf8kctDNo130_provenance.
- NP742988.RA9mqeWn0NXH1DASeEQrB0m-0XvjshAYghwZzf8kctDNo130_assertion SIO_000772 19651702 NP742988.RA9mqeWn0NXH1DASeEQrB0m-0XvjshAYghwZzf8kctDNo130_provenance.
- NP742988.RA9mqeWn0NXH1DASeEQrB0m-0XvjshAYghwZzf8kctDNo130_assertion wasDerivedFrom befree-20140225 NP742988.RA9mqeWn0NXH1DASeEQrB0m-0XvjshAYghwZzf8kctDNo130_provenance.
- NP742988.RA9mqeWn0NXH1DASeEQrB0m-0XvjshAYghwZzf8kctDNo130_assertion wasGeneratedBy ECO_0000203 NP742988.RA9mqeWn0NXH1DASeEQrB0m-0XvjshAYghwZzf8kctDNo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP742988.RA9mqeWn0NXH1DASeEQrB0m-0XvjshAYghwZzf8kctDNo130_provenance.