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- source_evidence_literature type ECO_0000212 NP1294943.RAC3i3KMUPQpcMbjBN1alpRsm6b-RUKaVowm77kgLiJTk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1294943.RAC3i3KMUPQpcMbjBN1alpRsm6b-RUKaVowm77kgLiJTk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1294943.RAC3i3KMUPQpcMbjBN1alpRsm6b-RUKaVowm77kgLiJTk130_provenance.
- NP1294943.RAC3i3KMUPQpcMbjBN1alpRsm6b-RUKaVowm77kgLiJTk130_assertion description "[Interestingly, 50% of NS individuals with an NRAS mutation (including our family) present with lentigines and/or Caf�-au-lait spots.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1294943.RAC3i3KMUPQpcMbjBN1alpRsm6b-RUKaVowm77kgLiJTk130_provenance.
- NP1294943.RAC3i3KMUPQpcMbjBN1alpRsm6b-RUKaVowm77kgLiJTk130_assertion evidence source_evidence_literature NP1294943.RAC3i3KMUPQpcMbjBN1alpRsm6b-RUKaVowm77kgLiJTk130_provenance.
- NP1294943.RAC3i3KMUPQpcMbjBN1alpRsm6b-RUKaVowm77kgLiJTk130_assertion SIO_000772 26467218 NP1294943.RAC3i3KMUPQpcMbjBN1alpRsm6b-RUKaVowm77kgLiJTk130_provenance.
- NP1294943.RAC3i3KMUPQpcMbjBN1alpRsm6b-RUKaVowm77kgLiJTk130_assertion wasDerivedFrom befree-2016 NP1294943.RAC3i3KMUPQpcMbjBN1alpRsm6b-RUKaVowm77kgLiJTk130_provenance.
- NP1294943.RAC3i3KMUPQpcMbjBN1alpRsm6b-RUKaVowm77kgLiJTk130_assertion wasGeneratedBy ECO_0000203 NP1294943.RAC3i3KMUPQpcMbjBN1alpRsm6b-RUKaVowm77kgLiJTk130_provenance.
- befree-2016 importedOn "2016-02-19" NP1294943.RAC3i3KMUPQpcMbjBN1alpRsm6b-RUKaVowm77kgLiJTk130_provenance.