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- source_evidence_literature type ECO_0000212 NP939281.RAHrZWvXL1mFd4nRl_pUzIkR8yfC7ujmzjuf2tYDgVisI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP939281.RAHrZWvXL1mFd4nRl_pUzIkR8yfC7ujmzjuf2tYDgVisI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP939281.RAHrZWvXL1mFd4nRl_pUzIkR8yfC7ujmzjuf2tYDgVisI130_provenance.
- NP939281.RAHrZWvXL1mFd4nRl_pUzIkR8yfC7ujmzjuf2tYDgVisI130_assertion description "[We performed direct genotyping of INF2 in 16 index patients with Charcot-Marie-Tooth neuropathy and FSGS who did not have a mutation in PMP22 or MPZ, encoding peripheral myelin protein 22 and myelin protein zero, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP939281.RAHrZWvXL1mFd4nRl_pUzIkR8yfC7ujmzjuf2tYDgVisI130_provenance.
- NP939281.RAHrZWvXL1mFd4nRl_pUzIkR8yfC7ujmzjuf2tYDgVisI130_assertion evidence source_evidence_literature NP939281.RAHrZWvXL1mFd4nRl_pUzIkR8yfC7ujmzjuf2tYDgVisI130_provenance.
- NP939281.RAHrZWvXL1mFd4nRl_pUzIkR8yfC7ujmzjuf2tYDgVisI130_assertion SIO_000772 22187985 NP939281.RAHrZWvXL1mFd4nRl_pUzIkR8yfC7ujmzjuf2tYDgVisI130_provenance.
- NP939281.RAHrZWvXL1mFd4nRl_pUzIkR8yfC7ujmzjuf2tYDgVisI130_assertion wasDerivedFrom befree-20150227 NP939281.RAHrZWvXL1mFd4nRl_pUzIkR8yfC7ujmzjuf2tYDgVisI130_provenance.
- NP939281.RAHrZWvXL1mFd4nRl_pUzIkR8yfC7ujmzjuf2tYDgVisI130_assertion wasGeneratedBy ECO_0000203 NP939281.RAHrZWvXL1mFd4nRl_pUzIkR8yfC7ujmzjuf2tYDgVisI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP939281.RAHrZWvXL1mFd4nRl_pUzIkR8yfC7ujmzjuf2tYDgVisI130_provenance.