Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP700987.RAiF4eIBxryDAcDbg3SaHl5kLE-cHL83dgDQJ099bN5xY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP700987.RAiF4eIBxryDAcDbg3SaHl5kLE-cHL83dgDQJ099bN5xY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP700987.RAiF4eIBxryDAcDbg3SaHl5kLE-cHL83dgDQJ099bN5xY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP700987.RAiF4eIBxryDAcDbg3SaHl5kLE-cHL83dgDQJ099bN5xY130_provenance.
- NP700987.RAiF4eIBxryDAcDbg3SaHl5kLE-cHL83dgDQJ099bN5xY130_assertion description "[COL4A1 mutations can present in children with infantile hemiplegia/quadriplegia, stroke or epilepsy, and a motor disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP700987.RAiF4eIBxryDAcDbg3SaHl5kLE-cHL83dgDQJ099bN5xY130_provenance.
- NP700987.RAiF4eIBxryDAcDbg3SaHl5kLE-cHL83dgDQJ099bN5xY130_assertion evidence source_evidence_literature NP700987.RAiF4eIBxryDAcDbg3SaHl5kLE-cHL83dgDQJ099bN5xY130_provenance.
- NP700987.RAiF4eIBxryDAcDbg3SaHl5kLE-cHL83dgDQJ099bN5xY130_assertion SIO_000772 22574627 NP700987.RAiF4eIBxryDAcDbg3SaHl5kLE-cHL83dgDQJ099bN5xY130_provenance.
- NP700987.RAiF4eIBxryDAcDbg3SaHl5kLE-cHL83dgDQJ099bN5xY130_assertion wasDerivedFrom befree-20140225 NP700987.RAiF4eIBxryDAcDbg3SaHl5kLE-cHL83dgDQJ099bN5xY130_provenance.
- NP700987.RAiF4eIBxryDAcDbg3SaHl5kLE-cHL83dgDQJ099bN5xY130_assertion wasGeneratedBy ECO_0000203 NP700987.RAiF4eIBxryDAcDbg3SaHl5kLE-cHL83dgDQJ099bN5xY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP700987.RAiF4eIBxryDAcDbg3SaHl5kLE-cHL83dgDQJ099bN5xY130_provenance.