Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP875795.RAGhn_PM--FE0cIWvoiR6RCH6aGG80oBwsAxA_e9N8rLg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP875795.RAGhn_PM--FE0cIWvoiR6RCH6aGG80oBwsAxA_e9N8rLg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP875795.RAGhn_PM--FE0cIWvoiR6RCH6aGG80oBwsAxA_e9N8rLg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP875795.RAGhn_PM--FE0cIWvoiR6RCH6aGG80oBwsAxA_e9N8rLg130_provenance.
- NP875795.RAGhn_PM--FE0cIWvoiR6RCH6aGG80oBwsAxA_e9N8rLg130_assertion description "[This is the first report of a patient with partial trisomy 19p13.3 and partial monosomy p36.3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP875795.RAGhn_PM--FE0cIWvoiR6RCH6aGG80oBwsAxA_e9N8rLg130_provenance.
- NP875795.RAGhn_PM--FE0cIWvoiR6RCH6aGG80oBwsAxA_e9N8rLg130_assertion evidence source_evidence_literature NP875795.RAGhn_PM--FE0cIWvoiR6RCH6aGG80oBwsAxA_e9N8rLg130_provenance.
- NP875795.RAGhn_PM--FE0cIWvoiR6RCH6aGG80oBwsAxA_e9N8rLg130_assertion SIO_000772 19610110 NP875795.RAGhn_PM--FE0cIWvoiR6RCH6aGG80oBwsAxA_e9N8rLg130_provenance.
- NP875795.RAGhn_PM--FE0cIWvoiR6RCH6aGG80oBwsAxA_e9N8rLg130_assertion wasDerivedFrom befree-20140225 NP875795.RAGhn_PM--FE0cIWvoiR6RCH6aGG80oBwsAxA_e9N8rLg130_provenance.
- NP875795.RAGhn_PM--FE0cIWvoiR6RCH6aGG80oBwsAxA_e9N8rLg130_assertion wasGeneratedBy ECO_0000203 NP875795.RAGhn_PM--FE0cIWvoiR6RCH6aGG80oBwsAxA_e9N8rLg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP875795.RAGhn_PM--FE0cIWvoiR6RCH6aGG80oBwsAxA_e9N8rLg130_provenance.