Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP187036.RAYrV7e_CHmftLvfPkaSuevyAmv7I7Vf8c6C1FCiIhAbc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP187036.RAYrV7e_CHmftLvfPkaSuevyAmv7I7Vf8c6C1FCiIhAbc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP187036.RAYrV7e_CHmftLvfPkaSuevyAmv7I7Vf8c6C1FCiIhAbc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP187036.RAYrV7e_CHmftLvfPkaSuevyAmv7I7Vf8c6C1FCiIhAbc130_provenance.
- NP187036.RAYrV7e_CHmftLvfPkaSuevyAmv7I7Vf8c6C1FCiIhAbc130_assertion description "[Holoprosencephaly, sacral anomalies, and situs ambiguus in an infant with partial monosomy 7q/trisomy 2p and SHH and HLXB9 haploinsufficiency..]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187036.RAYrV7e_CHmftLvfPkaSuevyAmv7I7Vf8c6C1FCiIhAbc130_provenance.
- NP187036.RAYrV7e_CHmftLvfPkaSuevyAmv7I7Vf8c6C1FCiIhAbc130_assertion evidence source_evidence_literature NP187036.RAYrV7e_CHmftLvfPkaSuevyAmv7I7Vf8c6C1FCiIhAbc130_provenance.
- NP187036.RAYrV7e_CHmftLvfPkaSuevyAmv7I7Vf8c6C1FCiIhAbc130_assertion SIO_000772 10852374 NP187036.RAYrV7e_CHmftLvfPkaSuevyAmv7I7Vf8c6C1FCiIhAbc130_provenance.
- NP187036.RAYrV7e_CHmftLvfPkaSuevyAmv7I7Vf8c6C1FCiIhAbc130_assertion wasDerivedFrom befree-20140225 NP187036.RAYrV7e_CHmftLvfPkaSuevyAmv7I7Vf8c6C1FCiIhAbc130_provenance.
- NP187036.RAYrV7e_CHmftLvfPkaSuevyAmv7I7Vf8c6C1FCiIhAbc130_assertion wasGeneratedBy ECO_0000203 NP187036.RAYrV7e_CHmftLvfPkaSuevyAmv7I7Vf8c6C1FCiIhAbc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP187036.RAYrV7e_CHmftLvfPkaSuevyAmv7I7Vf8c6C1FCiIhAbc130_provenance.