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- source_evidence_literature type ECO_0000212 NP794735.RADmsiMc10jOOCiY1qeY5Sf2uJ_BPNDq1ip_eUnu5zcfE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP794735.RADmsiMc10jOOCiY1qeY5Sf2uJ_BPNDq1ip_eUnu5zcfE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP794735.RADmsiMc10jOOCiY1qeY5Sf2uJ_BPNDq1ip_eUnu5zcfE130_provenance.
- NP794735.RADmsiMc10jOOCiY1qeY5Sf2uJ_BPNDq1ip_eUnu5zcfE130_assertion description "[Mutations in the human gene MCPH1 cause primary microcephaly associated with a unique cellular phenotype with premature chromosome condensation (PCC) in early G2 phase and delayed decondensation post-mitosis (PCC syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP794735.RADmsiMc10jOOCiY1qeY5Sf2uJ_BPNDq1ip_eUnu5zcfE130_provenance.
- NP794735.RADmsiMc10jOOCiY1qeY5Sf2uJ_BPNDq1ip_eUnu5zcfE130_assertion evidence source_evidence_literature NP794735.RADmsiMc10jOOCiY1qeY5Sf2uJ_BPNDq1ip_eUnu5zcfE130_provenance.
- NP794735.RADmsiMc10jOOCiY1qeY5Sf2uJ_BPNDq1ip_eUnu5zcfE130_assertion SIO_000772 20169082 NP794735.RADmsiMc10jOOCiY1qeY5Sf2uJ_BPNDq1ip_eUnu5zcfE130_provenance.
- NP794735.RADmsiMc10jOOCiY1qeY5Sf2uJ_BPNDq1ip_eUnu5zcfE130_assertion wasDerivedFrom befree-2016 NP794735.RADmsiMc10jOOCiY1qeY5Sf2uJ_BPNDq1ip_eUnu5zcfE130_provenance.
- NP794735.RADmsiMc10jOOCiY1qeY5Sf2uJ_BPNDq1ip_eUnu5zcfE130_assertion wasGeneratedBy ECO_0000203 NP794735.RADmsiMc10jOOCiY1qeY5Sf2uJ_BPNDq1ip_eUnu5zcfE130_provenance.
- befree-2016 importedOn "2016-02-19" NP794735.RADmsiMc10jOOCiY1qeY5Sf2uJ_BPNDq1ip_eUnu5zcfE130_provenance.