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- source_evidence_literature type ECO_0000212 NP156940.RA-2lX-V3RV32LXvqfjvjH8H0XmCLK9Tk9aqhx7A-FmME130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP156940.RA-2lX-V3RV32LXvqfjvjH8H0XmCLK9Tk9aqhx7A-FmME130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP156940.RA-2lX-V3RV32LXvqfjvjH8H0XmCLK9Tk9aqhx7A-FmME130_provenance.
- NP156940.RA-2lX-V3RV32LXvqfjvjH8H0XmCLK9Tk9aqhx7A-FmME130_assertion description "[SDHB protein expression was absent in all 102 phaeochromocytomas and paragangliomas with an SDHB, SDHC, or SDHD mutation, but was present in all 65 paraganglionic tumours related to multiple endocrine neoplasia type 2, von Hippel-Lindau disease, and neurofibromatosis type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP156940.RA-2lX-V3RV32LXvqfjvjH8H0XmCLK9Tk9aqhx7A-FmME130_provenance.
- NP156940.RA-2lX-V3RV32LXvqfjvjH8H0XmCLK9Tk9aqhx7A-FmME130_assertion evidence source_evidence_literature NP156940.RA-2lX-V3RV32LXvqfjvjH8H0XmCLK9Tk9aqhx7A-FmME130_provenance.
- NP156940.RA-2lX-V3RV32LXvqfjvjH8H0XmCLK9Tk9aqhx7A-FmME130_assertion SIO_000772 19576851 NP156940.RA-2lX-V3RV32LXvqfjvjH8H0XmCLK9Tk9aqhx7A-FmME130_provenance.
- NP156940.RA-2lX-V3RV32LXvqfjvjH8H0XmCLK9Tk9aqhx7A-FmME130_assertion wasDerivedFrom befree-20140225 NP156940.RA-2lX-V3RV32LXvqfjvjH8H0XmCLK9Tk9aqhx7A-FmME130_provenance.
- NP156940.RA-2lX-V3RV32LXvqfjvjH8H0XmCLK9Tk9aqhx7A-FmME130_assertion wasGeneratedBy ECO_0000203 NP156940.RA-2lX-V3RV32LXvqfjvjH8H0XmCLK9Tk9aqhx7A-FmME130_provenance.
- befree-20140225 importedOn "2014-02-25" NP156940.RA-2lX-V3RV32LXvqfjvjH8H0XmCLK9Tk9aqhx7A-FmME130_provenance.