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- source_evidence_literature type ECO_0000212 NP195607.RAMcsYebuJTgDCk99lN6GYXmK5Ekc1A0TqlRXov9cTgLQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP195607.RAMcsYebuJTgDCk99lN6GYXmK5Ekc1A0TqlRXov9cTgLQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP195607.RAMcsYebuJTgDCk99lN6GYXmK5Ekc1A0TqlRXov9cTgLQ130_provenance.
- NP195607.RAMcsYebuJTgDCk99lN6GYXmK5Ekc1A0TqlRXov9cTgLQ130_assertion description "[ZFHX1B may be an important gene for normal embryonic neural crest development/indicate that Hirschsprung's disease can be regarded as a congenital malformation/were located at exon 8 of ZFHX1B in 3 of 4 cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP195607.RAMcsYebuJTgDCk99lN6GYXmK5Ekc1A0TqlRXov9cTgLQ130_provenance.
- NP195607.RAMcsYebuJTgDCk99lN6GYXmK5Ekc1A0TqlRXov9cTgLQ130_assertion evidence source_evidence_literature NP195607.RAMcsYebuJTgDCk99lN6GYXmK5Ekc1A0TqlRXov9cTgLQ130_provenance.
- NP195607.RAMcsYebuJTgDCk99lN6GYXmK5Ekc1A0TqlRXov9cTgLQ130_assertion SIO_000772 12149685 NP195607.RAMcsYebuJTgDCk99lN6GYXmK5Ekc1A0TqlRXov9cTgLQ130_provenance.
- NP195607.RAMcsYebuJTgDCk99lN6GYXmK5Ekc1A0TqlRXov9cTgLQ130_assertion wasDerivedFrom lhgdn-20090331 NP195607.RAMcsYebuJTgDCk99lN6GYXmK5Ekc1A0TqlRXov9cTgLQ130_provenance.
- NP195607.RAMcsYebuJTgDCk99lN6GYXmK5Ekc1A0TqlRXov9cTgLQ130_assertion wasGeneratedBy ECO_0000203 NP195607.RAMcsYebuJTgDCk99lN6GYXmK5Ekc1A0TqlRXov9cTgLQ130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP195607.RAMcsYebuJTgDCk99lN6GYXmK5Ekc1A0TqlRXov9cTgLQ130_provenance.