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- source_evidence_literature type ECO_0000212 NP558429.RAa60kaGLdKyHEEWAmG0CrwhtD9u-kC34JPcpYrgX-CTo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP558429.RAa60kaGLdKyHEEWAmG0CrwhtD9u-kC34JPcpYrgX-CTo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP558429.RAa60kaGLdKyHEEWAmG0CrwhtD9u-kC34JPcpYrgX-CTo130_provenance.
- NP558429.RAa60kaGLdKyHEEWAmG0CrwhtD9u-kC34JPcpYrgX-CTo130_assertion description "[These findings suggest that mutations in MLH1 may underlie a subset of LCIS cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP558429.RAa60kaGLdKyHEEWAmG0CrwhtD9u-kC34JPcpYrgX-CTo130_provenance.
- NP558429.RAa60kaGLdKyHEEWAmG0CrwhtD9u-kC34JPcpYrgX-CTo130_assertion evidence source_evidence_literature NP558429.RAa60kaGLdKyHEEWAmG0CrwhtD9u-kC34JPcpYrgX-CTo130_provenance.
- NP558429.RAa60kaGLdKyHEEWAmG0CrwhtD9u-kC34JPcpYrgX-CTo130_assertion SIO_000772 11369138 NP558429.RAa60kaGLdKyHEEWAmG0CrwhtD9u-kC34JPcpYrgX-CTo130_provenance.
- NP558429.RAa60kaGLdKyHEEWAmG0CrwhtD9u-kC34JPcpYrgX-CTo130_assertion wasDerivedFrom befree-20150227 NP558429.RAa60kaGLdKyHEEWAmG0CrwhtD9u-kC34JPcpYrgX-CTo130_provenance.
- NP558429.RAa60kaGLdKyHEEWAmG0CrwhtD9u-kC34JPcpYrgX-CTo130_assertion wasGeneratedBy ECO_0000203 NP558429.RAa60kaGLdKyHEEWAmG0CrwhtD9u-kC34JPcpYrgX-CTo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP558429.RAa60kaGLdKyHEEWAmG0CrwhtD9u-kC34JPcpYrgX-CTo130_provenance.