Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1293714.RA8cw7EuhRzxg_XW37uu3jblLDKtDUoMxTgXHF-AP8OYE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1293714.RA8cw7EuhRzxg_XW37uu3jblLDKtDUoMxTgXHF-AP8OYE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1293714.RA8cw7EuhRzxg_XW37uu3jblLDKtDUoMxTgXHF-AP8OYE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1293714.RA8cw7EuhRzxg_XW37uu3jblLDKtDUoMxTgXHF-AP8OYE130_provenance.
- NP1293714.RA8cw7EuhRzxg_XW37uu3jblLDKtDUoMxTgXHF-AP8OYE130_assertion description "[Human FANCM has been linked to Fanconi anemia, a syndrome characterized by cancer predisposition, developmental disorder, and bone marrow failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1293714.RA8cw7EuhRzxg_XW37uu3jblLDKtDUoMxTgXHF-AP8OYE130_provenance.
- NP1293714.RA8cw7EuhRzxg_XW37uu3jblLDKtDUoMxTgXHF-AP8OYE130_assertion evidence source_evidence_literature NP1293714.RA8cw7EuhRzxg_XW37uu3jblLDKtDUoMxTgXHF-AP8OYE130_provenance.
- NP1293714.RA8cw7EuhRzxg_XW37uu3jblLDKtDUoMxTgXHF-AP8OYE130_assertion SIO_000772 26341555 NP1293714.RA8cw7EuhRzxg_XW37uu3jblLDKtDUoMxTgXHF-AP8OYE130_provenance.
- NP1293714.RA8cw7EuhRzxg_XW37uu3jblLDKtDUoMxTgXHF-AP8OYE130_assertion wasDerivedFrom befree-2016 NP1293714.RA8cw7EuhRzxg_XW37uu3jblLDKtDUoMxTgXHF-AP8OYE130_provenance.
- NP1293714.RA8cw7EuhRzxg_XW37uu3jblLDKtDUoMxTgXHF-AP8OYE130_assertion wasGeneratedBy ECO_0000203 NP1293714.RA8cw7EuhRzxg_XW37uu3jblLDKtDUoMxTgXHF-AP8OYE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1293714.RA8cw7EuhRzxg_XW37uu3jblLDKtDUoMxTgXHF-AP8OYE130_provenance.