Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP412125.RAA2tvhsk0A-nxmYB1iTVDsXrzwgYqi3dYTYGVnBz6Z14130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP412125.RAA2tvhsk0A-nxmYB1iTVDsXrzwgYqi3dYTYGVnBz6Z14130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP412125.RAA2tvhsk0A-nxmYB1iTVDsXrzwgYqi3dYTYGVnBz6Z14130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP412125.RAA2tvhsk0A-nxmYB1iTVDsXrzwgYqi3dYTYGVnBz6Z14130_provenance.
- NP412125.RAA2tvhsk0A-nxmYB1iTVDsXrzwgYqi3dYTYGVnBz6Z14130_assertion description "[Identification of splicing mutations of the last nucleotides of exons, a nonsense mutation, and a missense mutation of the XPAC gene as causes of group A xeroderma pigmentosum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP412125.RAA2tvhsk0A-nxmYB1iTVDsXrzwgYqi3dYTYGVnBz6Z14130_provenance.
- NP412125.RAA2tvhsk0A-nxmYB1iTVDsXrzwgYqi3dYTYGVnBz6Z14130_assertion evidence source_evidence_literature NP412125.RAA2tvhsk0A-nxmYB1iTVDsXrzwgYqi3dYTYGVnBz6Z14130_provenance.
- NP412125.RAA2tvhsk0A-nxmYB1iTVDsXrzwgYqi3dYTYGVnBz6Z14130_assertion SIO_000772 1372103 NP412125.RAA2tvhsk0A-nxmYB1iTVDsXrzwgYqi3dYTYGVnBz6Z14130_provenance.
- NP412125.RAA2tvhsk0A-nxmYB1iTVDsXrzwgYqi3dYTYGVnBz6Z14130_assertion wasDerivedFrom befree-2016 NP412125.RAA2tvhsk0A-nxmYB1iTVDsXrzwgYqi3dYTYGVnBz6Z14130_provenance.
- NP412125.RAA2tvhsk0A-nxmYB1iTVDsXrzwgYqi3dYTYGVnBz6Z14130_assertion wasGeneratedBy ECO_0000203 NP412125.RAA2tvhsk0A-nxmYB1iTVDsXrzwgYqi3dYTYGVnBz6Z14130_provenance.
- befree-2016 importedOn "2016-02-19" NP412125.RAA2tvhsk0A-nxmYB1iTVDsXrzwgYqi3dYTYGVnBz6Z14130_provenance.