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- source_evidence_literature type ECO_0000212 NP960213.RAMVbyFy5TYV58ew_Rvbf1_5p-ywIejwrYmQ5W8OmcI88130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP960213.RAMVbyFy5TYV58ew_Rvbf1_5p-ywIejwrYmQ5W8OmcI88130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP960213.RAMVbyFy5TYV58ew_Rvbf1_5p-ywIejwrYmQ5W8OmcI88130_provenance.
- befree-2016 importedOn "2016-02-19" NP960213.RAMVbyFy5TYV58ew_Rvbf1_5p-ywIejwrYmQ5W8OmcI88130_provenance.
- NP960213.RAMVbyFy5TYV58ew_Rvbf1_5p-ywIejwrYmQ5W8OmcI88130_assertion wasGeneratedBy ECO_0000203 NP960213.RAMVbyFy5TYV58ew_Rvbf1_5p-ywIejwrYmQ5W8OmcI88130_provenance.
- NP960213.RAMVbyFy5TYV58ew_Rvbf1_5p-ywIejwrYmQ5W8OmcI88130_assertion wasDerivedFrom befree-2016 NP960213.RAMVbyFy5TYV58ew_Rvbf1_5p-ywIejwrYmQ5W8OmcI88130_provenance.
- NP960213.RAMVbyFy5TYV58ew_Rvbf1_5p-ywIejwrYmQ5W8OmcI88130_assertion SIO_000772 22326621 NP960213.RAMVbyFy5TYV58ew_Rvbf1_5p-ywIejwrYmQ5W8OmcI88130_provenance.
- NP960213.RAMVbyFy5TYV58ew_Rvbf1_5p-ywIejwrYmQ5W8OmcI88130_assertion evidence source_evidence_literature NP960213.RAMVbyFy5TYV58ew_Rvbf1_5p-ywIejwrYmQ5W8OmcI88130_provenance.
- NP960213.RAMVbyFy5TYV58ew_Rvbf1_5p-ywIejwrYmQ5W8OmcI88130_assertion description "[In addition, Boc, but not Cdon, mediates axon guidance information provided by Hh in specific neuronal populations, whereas mutations in the CDON cause holoprosencephaly, a human congenital anomaly defined by forebrain midline defects prominently associated with diminished Hh pathway activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP960213.RAMVbyFy5TYV58ew_Rvbf1_5p-ywIejwrYmQ5W8OmcI88130_provenance.