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- NP745799.RAVpgVI3CnwcQVRv3fGB9nHzext56sD--UlYEkGKnuddc130_assertion type Assertion NP745799.RAVpgVI3CnwcQVRv3fGB9nHzext56sD--UlYEkGKnuddc130_head.
- NP745799.RAVpgVI3CnwcQVRv3fGB9nHzext56sD--UlYEkGKnuddc130_assertion wasGeneratedBy ECO_0000203 NP745799.RAVpgVI3CnwcQVRv3fGB9nHzext56sD--UlYEkGKnuddc130_provenance.
- NP745799.RAVpgVI3CnwcQVRv3fGB9nHzext56sD--UlYEkGKnuddc130_assertion wasDerivedFrom befree-2016 NP745799.RAVpgVI3CnwcQVRv3fGB9nHzext56sD--UlYEkGKnuddc130_provenance.
- NP745799.RAVpgVI3CnwcQVRv3fGB9nHzext56sD--UlYEkGKnuddc130_assertion SIO_000772 19533801 NP745799.RAVpgVI3CnwcQVRv3fGB9nHzext56sD--UlYEkGKnuddc130_provenance.
- NP745799.RAVpgVI3CnwcQVRv3fGB9nHzext56sD--UlYEkGKnuddc130_assertion evidence source_evidence_literature NP745799.RAVpgVI3CnwcQVRv3fGB9nHzext56sD--UlYEkGKnuddc130_provenance.
- NP745799.RAVpgVI3CnwcQVRv3fGB9nHzext56sD--UlYEkGKnuddc130_assertion description "[We have identified the known c.1022 + 1G>A SUFU germ line splicing mutation in a family that was PTCH1-negative and who had signs and symptoms of GS, including medulloblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP745799.RAVpgVI3CnwcQVRv3fGB9nHzext56sD--UlYEkGKnuddc130_provenance.