Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP558312.RA1MfWnWiFpgf-dQfviBxrzXccsqikIc01GUsgF8BvI0g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP558312.RA1MfWnWiFpgf-dQfviBxrzXccsqikIc01GUsgF8BvI0g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP558312.RA1MfWnWiFpgf-dQfviBxrzXccsqikIc01GUsgF8BvI0g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP558312.RA1MfWnWiFpgf-dQfviBxrzXccsqikIc01GUsgF8BvI0g130_provenance.
- NP558312.RA1MfWnWiFpgf-dQfviBxrzXccsqikIc01GUsgF8BvI0g130_assertion description "[The other mutation detected in MLH1 was a TAC-->TAA substitution codon 750 (exon 19) creating a stop codon, predicted to generate a truncated protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP558312.RA1MfWnWiFpgf-dQfviBxrzXccsqikIc01GUsgF8BvI0g130_provenance.
- NP558312.RA1MfWnWiFpgf-dQfviBxrzXccsqikIc01GUsgF8BvI0g130_assertion evidence source_evidence_literature NP558312.RA1MfWnWiFpgf-dQfviBxrzXccsqikIc01GUsgF8BvI0g130_provenance.
- NP558312.RA1MfWnWiFpgf-dQfviBxrzXccsqikIc01GUsgF8BvI0g130_assertion SIO_000772 11369138 NP558312.RA1MfWnWiFpgf-dQfviBxrzXccsqikIc01GUsgF8BvI0g130_provenance.
- NP558312.RA1MfWnWiFpgf-dQfviBxrzXccsqikIc01GUsgF8BvI0g130_assertion wasDerivedFrom befree-20150227 NP558312.RA1MfWnWiFpgf-dQfviBxrzXccsqikIc01GUsgF8BvI0g130_provenance.
- NP558312.RA1MfWnWiFpgf-dQfviBxrzXccsqikIc01GUsgF8BvI0g130_assertion wasGeneratedBy ECO_0000203 NP558312.RA1MfWnWiFpgf-dQfviBxrzXccsqikIc01GUsgF8BvI0g130_provenance.
- befree-20150227 importedOn "2015-02-27" NP558312.RA1MfWnWiFpgf-dQfviBxrzXccsqikIc01GUsgF8BvI0g130_provenance.