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- source_evidence_literature type ECO_0000212 NP960737.RAcIePv7MJgNPrl6PqNq5TdAB_5PwQL9UJVJVlap0VAtk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP960737.RAcIePv7MJgNPrl6PqNq5TdAB_5PwQL9UJVJVlap0VAtk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP960737.RAcIePv7MJgNPrl6PqNq5TdAB_5PwQL9UJVJVlap0VAtk130_provenance.
- NP960737.RAcIePv7MJgNPrl6PqNq5TdAB_5PwQL9UJVJVlap0VAtk130_assertion description "[Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP960737.RAcIePv7MJgNPrl6PqNq5TdAB_5PwQL9UJVJVlap0VAtk130_provenance.
- NP960737.RAcIePv7MJgNPrl6PqNq5TdAB_5PwQL9UJVJVlap0VAtk130_assertion evidence source_evidence_literature NP960737.RAcIePv7MJgNPrl6PqNq5TdAB_5PwQL9UJVJVlap0VAtk130_provenance.
- NP960737.RAcIePv7MJgNPrl6PqNq5TdAB_5PwQL9UJVJVlap0VAtk130_assertion SIO_000772 19508969 NP960737.RAcIePv7MJgNPrl6PqNq5TdAB_5PwQL9UJVJVlap0VAtk130_provenance.
- NP960737.RAcIePv7MJgNPrl6PqNq5TdAB_5PwQL9UJVJVlap0VAtk130_assertion wasDerivedFrom befree-20150227 NP960737.RAcIePv7MJgNPrl6PqNq5TdAB_5PwQL9UJVJVlap0VAtk130_provenance.
- NP960737.RAcIePv7MJgNPrl6PqNq5TdAB_5PwQL9UJVJVlap0VAtk130_assertion wasGeneratedBy ECO_0000203 NP960737.RAcIePv7MJgNPrl6PqNq5TdAB_5PwQL9UJVJVlap0VAtk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP960737.RAcIePv7MJgNPrl6PqNq5TdAB_5PwQL9UJVJVlap0VAtk130_provenance.