Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP255484.RAU6X18VsnV4cIG3Sbimoj0cMYFuAdNm8zG-QZ9Qg53Vw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP255484.RAU6X18VsnV4cIG3Sbimoj0cMYFuAdNm8zG-QZ9Qg53Vw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP255484.RAU6X18VsnV4cIG3Sbimoj0cMYFuAdNm8zG-QZ9Qg53Vw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP255484.RAU6X18VsnV4cIG3Sbimoj0cMYFuAdNm8zG-QZ9Qg53Vw130_provenance.
- NP255484.RAU6X18VsnV4cIG3Sbimoj0cMYFuAdNm8zG-QZ9Qg53Vw130_assertion description "[Although medulloblastoma is a component of Turcot syndrome with demonstrated APC mutations, APC gene deletions appear to be absent or very uncommon in patients with sporadic and NBCCS-associated medulloblastomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP255484.RAU6X18VsnV4cIG3Sbimoj0cMYFuAdNm8zG-QZ9Qg53Vw130_provenance.
- NP255484.RAU6X18VsnV4cIG3Sbimoj0cMYFuAdNm8zG-QZ9Qg53Vw130_assertion evidence source_evidence_literature NP255484.RAU6X18VsnV4cIG3Sbimoj0cMYFuAdNm8zG-QZ9Qg53Vw130_provenance.
- NP255484.RAU6X18VsnV4cIG3Sbimoj0cMYFuAdNm8zG-QZ9Qg53Vw130_assertion SIO_000772 10375116 NP255484.RAU6X18VsnV4cIG3Sbimoj0cMYFuAdNm8zG-QZ9Qg53Vw130_provenance.
- NP255484.RAU6X18VsnV4cIG3Sbimoj0cMYFuAdNm8zG-QZ9Qg53Vw130_assertion wasDerivedFrom befree-2016 NP255484.RAU6X18VsnV4cIG3Sbimoj0cMYFuAdNm8zG-QZ9Qg53Vw130_provenance.
- NP255484.RAU6X18VsnV4cIG3Sbimoj0cMYFuAdNm8zG-QZ9Qg53Vw130_assertion wasGeneratedBy ECO_0000203 NP255484.RAU6X18VsnV4cIG3Sbimoj0cMYFuAdNm8zG-QZ9Qg53Vw130_provenance.
- befree-2016 importedOn "2016-02-19" NP255484.RAU6X18VsnV4cIG3Sbimoj0cMYFuAdNm8zG-QZ9Qg53Vw130_provenance.