Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP931599.RA5IO9dLtwe-wBu8ZP_mldCdO4LsEaKGtsyD3Z4Tu4fIo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP931599.RA5IO9dLtwe-wBu8ZP_mldCdO4LsEaKGtsyD3Z4Tu4fIo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP931599.RA5IO9dLtwe-wBu8ZP_mldCdO4LsEaKGtsyD3Z4Tu4fIo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP931599.RA5IO9dLtwe-wBu8ZP_mldCdO4LsEaKGtsyD3Z4Tu4fIo130_provenance.
- NP931599.RA5IO9dLtwe-wBu8ZP_mldCdO4LsEaKGtsyD3Z4Tu4fIo130_assertion description "[No mutations of the p51 gene causing amino acid substitutions or frameshifts were detected in either primary tumors or cancer cell lines by PCR-SSCP analysis of the entire coding region, although several genetic polymorphisms were detected in three samples.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP931599.RA5IO9dLtwe-wBu8ZP_mldCdO4LsEaKGtsyD3Z4Tu4fIo130_provenance.
- NP931599.RA5IO9dLtwe-wBu8ZP_mldCdO4LsEaKGtsyD3Z4Tu4fIo130_assertion evidence source_evidence_literature NP931599.RA5IO9dLtwe-wBu8ZP_mldCdO4LsEaKGtsyD3Z4Tu4fIo130_provenance.
- NP931599.RA5IO9dLtwe-wBu8ZP_mldCdO4LsEaKGtsyD3Z4Tu4fIo130_assertion SIO_000772 11179485 NP931599.RA5IO9dLtwe-wBu8ZP_mldCdO4LsEaKGtsyD3Z4Tu4fIo130_provenance.
- NP931599.RA5IO9dLtwe-wBu8ZP_mldCdO4LsEaKGtsyD3Z4Tu4fIo130_assertion wasDerivedFrom befree-20150227 NP931599.RA5IO9dLtwe-wBu8ZP_mldCdO4LsEaKGtsyD3Z4Tu4fIo130_provenance.
- NP931599.RA5IO9dLtwe-wBu8ZP_mldCdO4LsEaKGtsyD3Z4Tu4fIo130_assertion wasGeneratedBy ECO_0000203 NP931599.RA5IO9dLtwe-wBu8ZP_mldCdO4LsEaKGtsyD3Z4Tu4fIo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP931599.RA5IO9dLtwe-wBu8ZP_mldCdO4LsEaKGtsyD3Z4Tu4fIo130_provenance.