Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP759507.RAlTJ-0xoY6vXSkV6SXsHjMaBxiHeWPrq14BRTV9YW6lE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP759507.RAlTJ-0xoY6vXSkV6SXsHjMaBxiHeWPrq14BRTV9YW6lE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP759507.RAlTJ-0xoY6vXSkV6SXsHjMaBxiHeWPrq14BRTV9YW6lE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP759507.RAlTJ-0xoY6vXSkV6SXsHjMaBxiHeWPrq14BRTV9YW6lE130_provenance.
- NP759507.RAlTJ-0xoY6vXSkV6SXsHjMaBxiHeWPrq14BRTV9YW6lE130_assertion description "[We conclude that germline mutations in PRKAR1A, an apparent tumour-suppressor gene, are responsible for the CNC phenotype in a subset of patients with this disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP759507.RAlTJ-0xoY6vXSkV6SXsHjMaBxiHeWPrq14BRTV9YW6lE130_provenance.
- NP759507.RAlTJ-0xoY6vXSkV6SXsHjMaBxiHeWPrq14BRTV9YW6lE130_assertion evidence source_evidence_literature NP759507.RAlTJ-0xoY6vXSkV6SXsHjMaBxiHeWPrq14BRTV9YW6lE130_provenance.
- NP759507.RAlTJ-0xoY6vXSkV6SXsHjMaBxiHeWPrq14BRTV9YW6lE130_assertion SIO_000772 10973256 NP759507.RAlTJ-0xoY6vXSkV6SXsHjMaBxiHeWPrq14BRTV9YW6lE130_provenance.
- NP759507.RAlTJ-0xoY6vXSkV6SXsHjMaBxiHeWPrq14BRTV9YW6lE130_assertion wasDerivedFrom befree-20150227 NP759507.RAlTJ-0xoY6vXSkV6SXsHjMaBxiHeWPrq14BRTV9YW6lE130_provenance.
- NP759507.RAlTJ-0xoY6vXSkV6SXsHjMaBxiHeWPrq14BRTV9YW6lE130_assertion wasGeneratedBy ECO_0000203 NP759507.RAlTJ-0xoY6vXSkV6SXsHjMaBxiHeWPrq14BRTV9YW6lE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP759507.RAlTJ-0xoY6vXSkV6SXsHjMaBxiHeWPrq14BRTV9YW6lE130_provenance.