Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP578851.RAY3ZwmTM1VhwPtMnbdko0dd-Zm2_7vxrNORjSLmepxqk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP578851.RAY3ZwmTM1VhwPtMnbdko0dd-Zm2_7vxrNORjSLmepxqk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP578851.RAY3ZwmTM1VhwPtMnbdko0dd-Zm2_7vxrNORjSLmepxqk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP578851.RAY3ZwmTM1VhwPtMnbdko0dd-Zm2_7vxrNORjSLmepxqk130_provenance.
- NP578851.RAY3ZwmTM1VhwPtMnbdko0dd-Zm2_7vxrNORjSLmepxqk130_assertion description "[Exon deletions in SPG4 are as frequent as point mutations, and SPG4 is responsible for 40% of AD-HSP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP578851.RAY3ZwmTM1VhwPtMnbdko0dd-Zm2_7vxrNORjSLmepxqk130_provenance.
- NP578851.RAY3ZwmTM1VhwPtMnbdko0dd-Zm2_7vxrNORjSLmepxqk130_assertion evidence source_evidence_literature NP578851.RAY3ZwmTM1VhwPtMnbdko0dd-Zm2_7vxrNORjSLmepxqk130_provenance.
- NP578851.RAY3ZwmTM1VhwPtMnbdko0dd-Zm2_7vxrNORjSLmepxqk130_assertion SIO_000772 17098887 NP578851.RAY3ZwmTM1VhwPtMnbdko0dd-Zm2_7vxrNORjSLmepxqk130_provenance.
- NP578851.RAY3ZwmTM1VhwPtMnbdko0dd-Zm2_7vxrNORjSLmepxqk130_assertion wasDerivedFrom befree-2016 NP578851.RAY3ZwmTM1VhwPtMnbdko0dd-Zm2_7vxrNORjSLmepxqk130_provenance.
- NP578851.RAY3ZwmTM1VhwPtMnbdko0dd-Zm2_7vxrNORjSLmepxqk130_assertion wasGeneratedBy ECO_0000203 NP578851.RAY3ZwmTM1VhwPtMnbdko0dd-Zm2_7vxrNORjSLmepxqk130_provenance.
- befree-2016 importedOn "2016-02-19" NP578851.RAY3ZwmTM1VhwPtMnbdko0dd-Zm2_7vxrNORjSLmepxqk130_provenance.