Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP882870.RAIeNS1s3YPWxx1i_rdwpvvetpVDhO_EIVeGKzC7GMGBM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP882870.RAIeNS1s3YPWxx1i_rdwpvvetpVDhO_EIVeGKzC7GMGBM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP882870.RAIeNS1s3YPWxx1i_rdwpvvetpVDhO_EIVeGKzC7GMGBM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP882870.RAIeNS1s3YPWxx1i_rdwpvvetpVDhO_EIVeGKzC7GMGBM130_provenance.
- NP882870.RAIeNS1s3YPWxx1i_rdwpvvetpVDhO_EIVeGKzC7GMGBM130_assertion description "[A p53 missense mutation was detected at codon 161 (GCC-->ACC, Ala-->Thr) in only one oligoastrocytoma without allelic loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP882870.RAIeNS1s3YPWxx1i_rdwpvvetpVDhO_EIVeGKzC7GMGBM130_provenance.
- NP882870.RAIeNS1s3YPWxx1i_rdwpvvetpVDhO_EIVeGKzC7GMGBM130_assertion evidence source_evidence_literature NP882870.RAIeNS1s3YPWxx1i_rdwpvvetpVDhO_EIVeGKzC7GMGBM130_provenance.
- NP882870.RAIeNS1s3YPWxx1i_rdwpvvetpVDhO_EIVeGKzC7GMGBM130_assertion SIO_000772 12507133 NP882870.RAIeNS1s3YPWxx1i_rdwpvvetpVDhO_EIVeGKzC7GMGBM130_provenance.
- NP882870.RAIeNS1s3YPWxx1i_rdwpvvetpVDhO_EIVeGKzC7GMGBM130_assertion wasDerivedFrom befree-20140225 NP882870.RAIeNS1s3YPWxx1i_rdwpvvetpVDhO_EIVeGKzC7GMGBM130_provenance.
- NP882870.RAIeNS1s3YPWxx1i_rdwpvvetpVDhO_EIVeGKzC7GMGBM130_assertion wasGeneratedBy ECO_0000203 NP882870.RAIeNS1s3YPWxx1i_rdwpvvetpVDhO_EIVeGKzC7GMGBM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP882870.RAIeNS1s3YPWxx1i_rdwpvvetpVDhO_EIVeGKzC7GMGBM130_provenance.