Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP318630.RA7IaIsD81Q6qX5TNGDA7TYbCyZ9SeKA0U6rWE2TUA9gQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP318630.RA7IaIsD81Q6qX5TNGDA7TYbCyZ9SeKA0U6rWE2TUA9gQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP318630.RA7IaIsD81Q6qX5TNGDA7TYbCyZ9SeKA0U6rWE2TUA9gQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP318630.RA7IaIsD81Q6qX5TNGDA7TYbCyZ9SeKA0U6rWE2TUA9gQ130_provenance.
- NP318630.RA7IaIsD81Q6qX5TNGDA7TYbCyZ9SeKA0U6rWE2TUA9gQ130_assertion description "[These findings suggest that mutations in MLH1 may underlie a subset of LCIS cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP318630.RA7IaIsD81Q6qX5TNGDA7TYbCyZ9SeKA0U6rWE2TUA9gQ130_provenance.
- NP318630.RA7IaIsD81Q6qX5TNGDA7TYbCyZ9SeKA0U6rWE2TUA9gQ130_assertion evidence source_evidence_literature NP318630.RA7IaIsD81Q6qX5TNGDA7TYbCyZ9SeKA0U6rWE2TUA9gQ130_provenance.
- NP318630.RA7IaIsD81Q6qX5TNGDA7TYbCyZ9SeKA0U6rWE2TUA9gQ130_assertion SIO_000772 11369138 NP318630.RA7IaIsD81Q6qX5TNGDA7TYbCyZ9SeKA0U6rWE2TUA9gQ130_provenance.
- NP318630.RA7IaIsD81Q6qX5TNGDA7TYbCyZ9SeKA0U6rWE2TUA9gQ130_assertion wasDerivedFrom befree-2016 NP318630.RA7IaIsD81Q6qX5TNGDA7TYbCyZ9SeKA0U6rWE2TUA9gQ130_provenance.
- NP318630.RA7IaIsD81Q6qX5TNGDA7TYbCyZ9SeKA0U6rWE2TUA9gQ130_assertion wasGeneratedBy ECO_0000203 NP318630.RA7IaIsD81Q6qX5TNGDA7TYbCyZ9SeKA0U6rWE2TUA9gQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP318630.RA7IaIsD81Q6qX5TNGDA7TYbCyZ9SeKA0U6rWE2TUA9gQ130_provenance.