Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1290331.RANo0hI_P71dwtH3bBOjg-caULF0P3f6MI4bHXFdVP-vA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1290331.RANo0hI_P71dwtH3bBOjg-caULF0P3f6MI4bHXFdVP-vA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1290331.RANo0hI_P71dwtH3bBOjg-caULF0P3f6MI4bHXFdVP-vA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1290331.RANo0hI_P71dwtH3bBOjg-caULF0P3f6MI4bHXFdVP-vA130_provenance.
- NP1290331.RANo0hI_P71dwtH3bBOjg-caULF0P3f6MI4bHXFdVP-vA130_assertion description "[A novel deletion in the splice donor site of MLH1 exon 6 in a Japanese colon cancer patient with Lynch syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1290331.RANo0hI_P71dwtH3bBOjg-caULF0P3f6MI4bHXFdVP-vA130_provenance.
- NP1290331.RANo0hI_P71dwtH3bBOjg-caULF0P3f6MI4bHXFdVP-vA130_assertion evidence source_evidence_literature NP1290331.RANo0hI_P71dwtH3bBOjg-caULF0P3f6MI4bHXFdVP-vA130_provenance.
- NP1290331.RANo0hI_P71dwtH3bBOjg-caULF0P3f6MI4bHXFdVP-vA130_assertion SIO_000772 26185136 NP1290331.RANo0hI_P71dwtH3bBOjg-caULF0P3f6MI4bHXFdVP-vA130_provenance.
- NP1290331.RANo0hI_P71dwtH3bBOjg-caULF0P3f6MI4bHXFdVP-vA130_assertion wasDerivedFrom befree-2016 NP1290331.RANo0hI_P71dwtH3bBOjg-caULF0P3f6MI4bHXFdVP-vA130_provenance.
- NP1290331.RANo0hI_P71dwtH3bBOjg-caULF0P3f6MI4bHXFdVP-vA130_assertion wasGeneratedBy ECO_0000203 NP1290331.RANo0hI_P71dwtH3bBOjg-caULF0P3f6MI4bHXFdVP-vA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1290331.RANo0hI_P71dwtH3bBOjg-caULF0P3f6MI4bHXFdVP-vA130_provenance.