Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1232331.RADlOy3gXfLGmztwp085P2Ja_HzjSTi4YQeIA1V1hI-_o130_assertion> ?p ?o ?g. }
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- NP1232331.RADlOy3gXfLGmztwp085P2Ja_HzjSTi4YQeIA1V1hI-_o130_assertion type Assertion NP1232331.RADlOy3gXfLGmztwp085P2Ja_HzjSTi4YQeIA1V1hI-_o130_head.
- NP1232331.RADlOy3gXfLGmztwp085P2Ja_HzjSTi4YQeIA1V1hI-_o130_assertion description "[We also identified one heterozygous 6.5-Mb deletion encompassing OTX2 in a patient with bilateral anophthalmia and multiple pituitary hormone deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1232331.RADlOy3gXfLGmztwp085P2Ja_HzjSTi4YQeIA1V1hI-_o130_provenance.
- NP1232331.RADlOy3gXfLGmztwp085P2Ja_HzjSTi4YQeIA1V1hI-_o130_assertion evidence source_evidence_literature NP1232331.RADlOy3gXfLGmztwp085P2Ja_HzjSTi4YQeIA1V1hI-_o130_provenance.
- NP1232331.RADlOy3gXfLGmztwp085P2Ja_HzjSTi4YQeIA1V1hI-_o130_assertion SIO_000772 25342853 NP1232331.RADlOy3gXfLGmztwp085P2Ja_HzjSTi4YQeIA1V1hI-_o130_provenance.
- NP1232331.RADlOy3gXfLGmztwp085P2Ja_HzjSTi4YQeIA1V1hI-_o130_assertion wasDerivedFrom befree-2016 NP1232331.RADlOy3gXfLGmztwp085P2Ja_HzjSTi4YQeIA1V1hI-_o130_provenance.
- NP1232331.RADlOy3gXfLGmztwp085P2Ja_HzjSTi4YQeIA1V1hI-_o130_assertion wasGeneratedBy ECO_0000203 NP1232331.RADlOy3gXfLGmztwp085P2Ja_HzjSTi4YQeIA1V1hI-_o130_provenance.