Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP656040.RAAPhezBp_OBRVPnIpwWLwrlJldVnY0fUmMk39vI2MFLk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP656040.RAAPhezBp_OBRVPnIpwWLwrlJldVnY0fUmMk39vI2MFLk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP656040.RAAPhezBp_OBRVPnIpwWLwrlJldVnY0fUmMk39vI2MFLk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP656040.RAAPhezBp_OBRVPnIpwWLwrlJldVnY0fUmMk39vI2MFLk130_provenance.
- NP656040.RAAPhezBp_OBRVPnIpwWLwrlJldVnY0fUmMk39vI2MFLk130_assertion wasGeneratedBy ECO_0000203 NP656040.RAAPhezBp_OBRVPnIpwWLwrlJldVnY0fUmMk39vI2MFLk130_provenance.
- NP656040.RAAPhezBp_OBRVPnIpwWLwrlJldVnY0fUmMk39vI2MFLk130_assertion wasDerivedFrom befree-20140225 NP656040.RAAPhezBp_OBRVPnIpwWLwrlJldVnY0fUmMk39vI2MFLk130_provenance.
- NP656040.RAAPhezBp_OBRVPnIpwWLwrlJldVnY0fUmMk39vI2MFLk130_assertion SIO_000772 18460397 NP656040.RAAPhezBp_OBRVPnIpwWLwrlJldVnY0fUmMk39vI2MFLk130_provenance.
- NP656040.RAAPhezBp_OBRVPnIpwWLwrlJldVnY0fUmMk39vI2MFLk130_assertion evidence source_evidence_literature NP656040.RAAPhezBp_OBRVPnIpwWLwrlJldVnY0fUmMk39vI2MFLk130_provenance.
- NP656040.RAAPhezBp_OBRVPnIpwWLwrlJldVnY0fUmMk39vI2MFLk130_assertion description "[Seemingly identical pathogenic PTEN mutations have been observed in patients with CS and BRRS, as well as in patients with incomplete features of CS, referred to as CS-like (CSL) patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP656040.RAAPhezBp_OBRVPnIpwWLwrlJldVnY0fUmMk39vI2MFLk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP656040.RAAPhezBp_OBRVPnIpwWLwrlJldVnY0fUmMk39vI2MFLk130_provenance.