Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1327009.RA8bI94rvrWT3RZjAUxrrHapC5fNbyD7sgqVmFTBwnfe4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1327009.RA8bI94rvrWT3RZjAUxrrHapC5fNbyD7sgqVmFTBwnfe4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1327009.RA8bI94rvrWT3RZjAUxrrHapC5fNbyD7sgqVmFTBwnfe4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1327009.RA8bI94rvrWT3RZjAUxrrHapC5fNbyD7sgqVmFTBwnfe4130_provenance.
- NP1327009.RA8bI94rvrWT3RZjAUxrrHapC5fNbyD7sgqVmFTBwnfe4130_assertion description "[However, familial forms of ALS have been described--autosomal dominant forms (ALS1, ALS3), clinically indistinguishable from the sporadic form, and autosomal recessive forms with early onset and slower progression of symptoms (ALS2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1327009.RA8bI94rvrWT3RZjAUxrrHapC5fNbyD7sgqVmFTBwnfe4130_provenance.
- NP1327009.RA8bI94rvrWT3RZjAUxrrHapC5fNbyD7sgqVmFTBwnfe4130_assertion evidence source_evidence_literature NP1327009.RA8bI94rvrWT3RZjAUxrrHapC5fNbyD7sgqVmFTBwnfe4130_provenance.
- NP1327009.RA8bI94rvrWT3RZjAUxrrHapC5fNbyD7sgqVmFTBwnfe4130_assertion SIO_000772 7920663 NP1327009.RA8bI94rvrWT3RZjAUxrrHapC5fNbyD7sgqVmFTBwnfe4130_provenance.
- NP1327009.RA8bI94rvrWT3RZjAUxrrHapC5fNbyD7sgqVmFTBwnfe4130_assertion wasDerivedFrom befree-2016 NP1327009.RA8bI94rvrWT3RZjAUxrrHapC5fNbyD7sgqVmFTBwnfe4130_provenance.
- NP1327009.RA8bI94rvrWT3RZjAUxrrHapC5fNbyD7sgqVmFTBwnfe4130_assertion wasGeneratedBy ECO_0000203 NP1327009.RA8bI94rvrWT3RZjAUxrrHapC5fNbyD7sgqVmFTBwnfe4130_provenance.
- befree-2016 importedOn "2016-02-19" NP1327009.RA8bI94rvrWT3RZjAUxrrHapC5fNbyD7sgqVmFTBwnfe4130_provenance.