Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP476208.RAeDF5Q2lE_HlOWZGvno4j0r4U96Cl1Jhqnm764hjb0VI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP476208.RAeDF5Q2lE_HlOWZGvno4j0r4U96Cl1Jhqnm764hjb0VI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP476208.RAeDF5Q2lE_HlOWZGvno4j0r4U96Cl1Jhqnm764hjb0VI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP476208.RAeDF5Q2lE_HlOWZGvno4j0r4U96Cl1Jhqnm764hjb0VI130_provenance.
- NP476208.RAeDF5Q2lE_HlOWZGvno4j0r4U96Cl1Jhqnm764hjb0VI130_assertion description "[Morphological abnormalities in axonal outgrowth and fasciculation manifest in several regions of the nervous system in necdin null mouse embryos, including axons of sympathetic, retinal ganglion cell, serotonergic and catecholaminergic neurons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP476208.RAeDF5Q2lE_HlOWZGvno4j0r4U96Cl1Jhqnm764hjb0VI130_provenance.
- NP476208.RAeDF5Q2lE_HlOWZGvno4j0r4U96Cl1Jhqnm764hjb0VI130_assertion evidence source_evidence_literature NP476208.RAeDF5Q2lE_HlOWZGvno4j0r4U96Cl1Jhqnm764hjb0VI130_provenance.
- NP476208.RAeDF5Q2lE_HlOWZGvno4j0r4U96Cl1Jhqnm764hjb0VI130_assertion SIO_000772 15649943 NP476208.RAeDF5Q2lE_HlOWZGvno4j0r4U96Cl1Jhqnm764hjb0VI130_provenance.
- NP476208.RAeDF5Q2lE_HlOWZGvno4j0r4U96Cl1Jhqnm764hjb0VI130_assertion wasDerivedFrom befree-2016 NP476208.RAeDF5Q2lE_HlOWZGvno4j0r4U96Cl1Jhqnm764hjb0VI130_provenance.
- NP476208.RAeDF5Q2lE_HlOWZGvno4j0r4U96Cl1Jhqnm764hjb0VI130_assertion wasGeneratedBy ECO_0000203 NP476208.RAeDF5Q2lE_HlOWZGvno4j0r4U96Cl1Jhqnm764hjb0VI130_provenance.
- befree-2016 importedOn "2016-02-19" NP476208.RAeDF5Q2lE_HlOWZGvno4j0r4U96Cl1Jhqnm764hjb0VI130_provenance.