Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP395924.RA3zXedMguSipBBWReT8i9hFtPZV1cSOCA-rVxuQg73NY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP395924.RA3zXedMguSipBBWReT8i9hFtPZV1cSOCA-rVxuQg73NY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP395924.RA3zXedMguSipBBWReT8i9hFtPZV1cSOCA-rVxuQg73NY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP395924.RA3zXedMguSipBBWReT8i9hFtPZV1cSOCA-rVxuQg73NY130_provenance.
- NP395924.RA3zXedMguSipBBWReT8i9hFtPZV1cSOCA-rVxuQg73NY130_assertion description "[A locus for AR WMS has recently been mapped to chromosome 19p13.3-p13.2 while mutation within the fibrillin-1 gene (15q21.1) was found in one AD WMS family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP395924.RA3zXedMguSipBBWReT8i9hFtPZV1cSOCA-rVxuQg73NY130_provenance.
- NP395924.RA3zXedMguSipBBWReT8i9hFtPZV1cSOCA-rVxuQg73NY130_assertion evidence source_evidence_literature NP395924.RA3zXedMguSipBBWReT8i9hFtPZV1cSOCA-rVxuQg73NY130_provenance.
- NP395924.RA3zXedMguSipBBWReT8i9hFtPZV1cSOCA-rVxuQg73NY130_assertion SIO_000772 14598350 NP395924.RA3zXedMguSipBBWReT8i9hFtPZV1cSOCA-rVxuQg73NY130_provenance.
- NP395924.RA3zXedMguSipBBWReT8i9hFtPZV1cSOCA-rVxuQg73NY130_assertion wasDerivedFrom befree-20150227 NP395924.RA3zXedMguSipBBWReT8i9hFtPZV1cSOCA-rVxuQg73NY130_provenance.
- NP395924.RA3zXedMguSipBBWReT8i9hFtPZV1cSOCA-rVxuQg73NY130_assertion wasGeneratedBy ECO_0000203 NP395924.RA3zXedMguSipBBWReT8i9hFtPZV1cSOCA-rVxuQg73NY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP395924.RA3zXedMguSipBBWReT8i9hFtPZV1cSOCA-rVxuQg73NY130_provenance.