Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP658037.RA65WkWrXxKBvNEpBtnuLtBhCniTT9ZMCDLvDAgWFB4hs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP658037.RA65WkWrXxKBvNEpBtnuLtBhCniTT9ZMCDLvDAgWFB4hs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP658037.RA65WkWrXxKBvNEpBtnuLtBhCniTT9ZMCDLvDAgWFB4hs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP658037.RA65WkWrXxKBvNEpBtnuLtBhCniTT9ZMCDLvDAgWFB4hs130_provenance.
- NP658037.RA65WkWrXxKBvNEpBtnuLtBhCniTT9ZMCDLvDAgWFB4hs130_assertion description "[These deletions are close to the APC and VHL genes that confer susceptibility to familial Adenomatous polyposis (OMIM #17510) and von-Hippel-Lindau syndrome (OMIM #193300), respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP658037.RA65WkWrXxKBvNEpBtnuLtBhCniTT9ZMCDLvDAgWFB4hs130_provenance.
- NP658037.RA65WkWrXxKBvNEpBtnuLtBhCniTT9ZMCDLvDAgWFB4hs130_assertion evidence source_evidence_literature NP658037.RA65WkWrXxKBvNEpBtnuLtBhCniTT9ZMCDLvDAgWFB4hs130_provenance.
- NP658037.RA65WkWrXxKBvNEpBtnuLtBhCniTT9ZMCDLvDAgWFB4hs130_assertion SIO_000772 17954272 NP658037.RA65WkWrXxKBvNEpBtnuLtBhCniTT9ZMCDLvDAgWFB4hs130_provenance.
- NP658037.RA65WkWrXxKBvNEpBtnuLtBhCniTT9ZMCDLvDAgWFB4hs130_assertion wasDerivedFrom befree-20140225 NP658037.RA65WkWrXxKBvNEpBtnuLtBhCniTT9ZMCDLvDAgWFB4hs130_provenance.
- NP658037.RA65WkWrXxKBvNEpBtnuLtBhCniTT9ZMCDLvDAgWFB4hs130_assertion wasGeneratedBy ECO_0000203 NP658037.RA65WkWrXxKBvNEpBtnuLtBhCniTT9ZMCDLvDAgWFB4hs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP658037.RA65WkWrXxKBvNEpBtnuLtBhCniTT9ZMCDLvDAgWFB4hs130_provenance.