Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP388931.RAGFE8D5ix7c_VCSTxzcyem5U0E53ZyJJlzOFXLv9gy7Y130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP388931.RAGFE8D5ix7c_VCSTxzcyem5U0E53ZyJJlzOFXLv9gy7Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP388931.RAGFE8D5ix7c_VCSTxzcyem5U0E53ZyJJlzOFXLv9gy7Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP388931.RAGFE8D5ix7c_VCSTxzcyem5U0E53ZyJJlzOFXLv9gy7Y130_provenance.
- NP388931.RAGFE8D5ix7c_VCSTxzcyem5U0E53ZyJJlzOFXLv9gy7Y130_assertion description "[Here, we describe the positional cloning of SCAMP5, CLIC4 and PPCDC as candidate genes for autism, starting from a person with idiopathic, sporadic autism carrying a de novo chromosomal translocation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP388931.RAGFE8D5ix7c_VCSTxzcyem5U0E53ZyJJlzOFXLv9gy7Y130_provenance.
- NP388931.RAGFE8D5ix7c_VCSTxzcyem5U0E53ZyJJlzOFXLv9gy7Y130_assertion evidence source_evidence_literature NP388931.RAGFE8D5ix7c_VCSTxzcyem5U0E53ZyJJlzOFXLv9gy7Y130_provenance.
- NP388931.RAGFE8D5ix7c_VCSTxzcyem5U0E53ZyJJlzOFXLv9gy7Y130_assertion SIO_000772 20071347 NP388931.RAGFE8D5ix7c_VCSTxzcyem5U0E53ZyJJlzOFXLv9gy7Y130_provenance.
- NP388931.RAGFE8D5ix7c_VCSTxzcyem5U0E53ZyJJlzOFXLv9gy7Y130_assertion wasDerivedFrom befree-20140225 NP388931.RAGFE8D5ix7c_VCSTxzcyem5U0E53ZyJJlzOFXLv9gy7Y130_provenance.
- NP388931.RAGFE8D5ix7c_VCSTxzcyem5U0E53ZyJJlzOFXLv9gy7Y130_assertion wasGeneratedBy ECO_0000203 NP388931.RAGFE8D5ix7c_VCSTxzcyem5U0E53ZyJJlzOFXLv9gy7Y130_provenance.
- befree-20140225 importedOn "2014-02-25" NP388931.RAGFE8D5ix7c_VCSTxzcyem5U0E53ZyJJlzOFXLv9gy7Y130_provenance.