Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP438540.RAXhuu5sJTe4APYb8N281p_usv6cuNCcbyNookZLe-1CE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP438540.RAXhuu5sJTe4APYb8N281p_usv6cuNCcbyNookZLe-1CE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP438540.RAXhuu5sJTe4APYb8N281p_usv6cuNCcbyNookZLe-1CE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP438540.RAXhuu5sJTe4APYb8N281p_usv6cuNCcbyNookZLe-1CE130_provenance.
- NP438540.RAXhuu5sJTe4APYb8N281p_usv6cuNCcbyNookZLe-1CE130_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." NP438540.RAXhuu5sJTe4APYb8N281p_usv6cuNCcbyNookZLe-1CE130_provenance.
- NP438540.RAXhuu5sJTe4APYb8N281p_usv6cuNCcbyNookZLe-1CE130_assertion evidence source_evidence_literature NP438540.RAXhuu5sJTe4APYb8N281p_usv6cuNCcbyNookZLe-1CE130_provenance.
- NP438540.RAXhuu5sJTe4APYb8N281p_usv6cuNCcbyNookZLe-1CE130_assertion SIO_000772 11369138 NP438540.RAXhuu5sJTe4APYb8N281p_usv6cuNCcbyNookZLe-1CE130_provenance.
- NP438540.RAXhuu5sJTe4APYb8N281p_usv6cuNCcbyNookZLe-1CE130_assertion wasDerivedFrom befree-20140225 NP438540.RAXhuu5sJTe4APYb8N281p_usv6cuNCcbyNookZLe-1CE130_provenance.
- NP438540.RAXhuu5sJTe4APYb8N281p_usv6cuNCcbyNookZLe-1CE130_assertion wasGeneratedBy ECO_0000203 NP438540.RAXhuu5sJTe4APYb8N281p_usv6cuNCcbyNookZLe-1CE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP438540.RAXhuu5sJTe4APYb8N281p_usv6cuNCcbyNookZLe-1CE130_provenance.